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Corporate Overview Argonaut Manufacturing Services Inc. is a contract manufacturing organization (CMO) headquartered in Carlsbad, CA with over 100,000 square feet of manufacturing space across four locations. The company is dedicated to serving highly innovative companies in the biopharmaceutical and molecular diagnostics industries. Argonaut is a full service, cost-effective partner, providing complete solutions in the areas of formulation, filling and final kitting of reagents and consumables. Argonaut provides quality and regulatory expertise to assure the highest in quality manufacturing and supply chain excellence. Benefits and Pay Range At Argonaut Manufacturing Services we value our employees and are proud to offer a comprehensive benefits package designed to support your well-being and financial future. Eligible employees enjoy: Medical, Dental, and Vision Insurance Company-Paid Life Insurance (1x Annual Salary) Voluntary Life Insurance Options Short-Term and Long-Term Disability Insurance Flexible Spending Account (FSA)Health Savings Account (HSA) 401(k) Retirement Plan with Company Matching 14 Days of Paid Time Off (PTO) 10 Paid Holidays Annually The pay range for this position is $195,000 - $205,000 annually. Actual compensation will be based on factors such as location, skills, education, experience, and other relevant qualifications. Position Overview The Director of Quality Control is responsible for leading and managing all aspects of laboratory operations within QC Chemistry and Microbiology programs. This role ensures compliance with Good Manufacturing Practices (GMP) and other regulatory requirements while supporting organizational growth initiatives. The Director will oversee daily operations, including scheduling, staffing, training, troubleshooting, and continuous improvement efforts. Additionally, this position plays a critical role in managing analytical method transfers, instrument qualification, deviation investigations, and CAPA implementation. The Director will collaborate closely with cross-functional teams, providing strategic leadership in quality control while maintaining high standards of compliance, efficiency, and data integrity. The ideal candidate will have extensive experience in regulatory compliance (ISO-13485, ISO 14971, GMP/GLP, QSR, ICH guidelines), audit management, and client communications. This individual will bring a hands-on leadership approach, fostering a culture of excellence, accountability, and continuous improvement within the Quality Control team. This role is 100% on-site position Monday - Friday 8 hours/day (excluding lunch break). Overtime, weekends and holidays may be required. Flexible start time between 7:00 am - 9:00 am with a consistent schedule. Exceptions to the schedule must be approved by the manager in advance. Responsibilities and Duties Lead and manage daily laboratory operations for QC Chemistry and Microbiology programs, ensuring compliance with SOPs, GMP, and safety regulations. Oversee scheduling, staffing, training, and troubleshooting to maintain efficient workflows and high-quality standards. Write and review protocols, reports, and investigation documentation, including deviations, OOS, CAPAs, and change controls. Manage analytical method transfers, including phase-appropriate qualification and validation of test methods. Direct instrument qualification (IOQ) and ensure proper placement and maintenance of analytical equipment. Develop and implement process improvements to enhance efficiency, compliance, and data integrity. Support strategic planning, team development, and professional growth initiatives. Ensure objective product quality assessments through accurate and timely data generation. Lead audits, client interactions, and regulatory inspections, providing technical expertise and compliance assurance. Recruit, mentor, and develop a high-performing quality control team, fostering a culture of accountability and excellence. Requirements and Qualifications Bachelor's, Master's, or Ph.D. in a Life Science discipline (e.g., Chemistry, Microbiology, Molecular Biology, or Biochemistry). 10+ years of progressively increasing leadership experience in the medical device or pharmaceutical industry. Proven track record in FDA-regulated environments, including direct involvement with audits from the FDA, regulatory agencies, and clients. Experience managing 3rd-party contract laboratories. Strong analytical background in Chemistry and Microbiology, with the ability to execute objective and thorough OOS (Out of Specification) and failure investigations. Experience in a growth-oriented, contract manufacturing organization with a focus on compliance. Demonstrated success in strategic planning, process improvements, and professional development initiatives. In-depth knowledge of ISO-13485, ISO 14971, GMP/GLP, QSR, ICH Q1A/Q2, and 21 CFR 820.30. Strong understanding of analytical method validation, stability programs, and CAPA implementation. Ability to manage IOQ activities related to analytical instrumentation placement and validation. Proven credibility as a leader with a "hands-on" management style. Strong negotiation skills to maximize value in client and regulatory discussions. Excellent oral and written communication skills, including experience engaging with clients during audits, tours, and meetings. Ability to recruit, mentor, and develop high-performing teams within budget constraints. High level of personal and professional integrity with the ability to work independently and collaboratively. Argonaut Manufacturing Services, Inc. is proud to be an equal opportunity employer committed to providing employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age or disability, or any other class protected by Federal, State or local laws. Argonaut complies will all employment eligibility verification requirements of the Immigration and Nationality Act and all must have the authorization to work in the US.
Job Description We’re here for one reason and one reason only – to cure cancer. Every moment is dedicated to developing treatments and every action moves us one step closer to our goal. We’ve made incredible scientific breakthroughs and our pioneering personalized CAR T-cell therapies have changed the paradigm. But we're not finished yet. Join Kite, as we make even bigger advances in cancer therapies, and help shape where our business and medical science goes next. We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Kite and help create more tomorrows. Job Description We are seeking a highly motivated individual to join us as a Quality Control Operation Specialist I reporting to the QC analytical Sr Manager. You will work with the Quality team in supporting our efforts in this exciting new area of cancer immunotherapy. As a QC Operations Specialist I at Gilead/Kite you will ... - Perform drug substance lot release, in‑process, and stability testing in a GMP environment, including PCR, cell‑based assays, flow cytometry and RVV/LVV stability testing. -Execute routine laboratory testing in a GMP environment and accurately document results using KLIMS, demonstrating the ability to navigate the system effectively. - Perform routine sampling and sample management activities, including sample aliquoting, shipping, and external submissions, while maintaining sample integrity, traceability, and chain of custody. -Manage daily sample and reagent operations, including inventory control, organization, and traceability in compliance with GMP/GDP requirements. - Conduct laboratory maintenance activities, including biosafety cabinet (BSC) cleaning, equipment cleaning, general lab upkeep, media preparation, reagent ordering, and laboratory stocking. - Adhere to all GMP and GDP standards, site procedures, and safety requirements to ensure compliance and data integrity. - Serve as a signed‑off reviewer for assigned documentation in accordance with training. - Assist in the execution of validation and verification activities following approved protocols and procedures. - Support quality system activities, including assistance with deviations, CAPAs, change actions, and other quality records under supervision. - Assist in the assembly and maintenance of data trending reports, including Quality Control Metrics to support continuous improvement and compliance monitoring. - Participate in and support training activities, including completion of required training and assistance with training documentation as needed. - Support document revision activities with appropriate oversight. -Capability to lift and move items weighing up to 50 lbs on an occasional basis - Perform additional duties as assigned. The salary range for this position is: $80,325.00 - $103,950.00. Kite considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans*. For additional benefits information, visit: https://www.gilead.com/careers/compensation-benefits-and-wellbeing * Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans. Kite is a biopharmaceutical company engaged in the development of innovative cancer immunotherapies with a goal of providing rapid, long-term durable response and eliminating the burden of chronic care. The company is focused on chimeric antigen receptor (CAR) and T cell receptor (TCR) engineered cell therapies designed to empower the immune system's ability to recognize and kill tumors. Kite is based in Santa Monica, CA. NOTICE: EMPLOYEE POLYGRAPH PROTECTION ACT YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT Kite Pharma will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, (c) consistent with the legal duty to furnish information; or (d) otherwise protected by law. Our environment respects individual differences and recognizes each employee as an integral member of our company. Our workforce reflects these values and celebrates the individuals who make up our growing team. Kite Pharma provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion. For Current Kite Pharma Employees and Contractors: Please apply via the Internal Career Opportunities portal in Workday.
*Overview* Join our dynamic team as a Stone Fabricator, Installer, or Helper and become a vital part of transforming raw materials into stunning, durable stone surfaces. This role offers an energetic environment where craftsmanship meets precision, and safety is always a top priority. Whether you're fabricating intricate stone pieces or assisting with installations on-site, you'll contribute to creating beautiful, high-quality finishes that elevate our clients’ spaces. We are dedicated to fostering a positive work atmosphere that encourages growth, skill development, and teamwork. *Duties* * Operate fabrication equipment such as saws, grinders, and machining tools to cut, shape, and polish stone materials with accuracy. * Measure and interpret dimensional specifications to ensure precise fabrication and installation. * Assist in the handling and transportation of heavy stone slabs using forklifts or other heavy equipment while adhering to safety standards. * Prepare work areas by setting up personal protective equipment (PPE), including respiratory protection and safety gear, to maintain a safe working environment. * Support installation teams by lifting, positioning, and securing stone pieces during on-site assembly. * Follow safety regulations diligently during all phases of fabrication and installation to prevent accidents or injuries. * Use hand tools and power tools effectively for cutting, grinding, polishing, and finishing stone surfaces. * Handle materials carefully in warehouse settings, ensuring proper storage and handling of heavy slabs and fabricated components. * Assist with welding or machining tasks as needed for custom fabrication projects. * Maintain cleanliness of work areas and equipment to ensure optimal operation and safety compliance. *Qualifications* * Prior experience in fabrication, manufacturing, construction, or warehouse environments is highly desirable. * Mechanical knowledge related to machinery operation and maintenance is a plus. * Ability to perform heavy lifting safely while following proper techniques. * Familiarity with safety standards in production environments, including PPE use and respiratory protection protocols. * Experience operating forklifts or other heavy equipment is preferred; certification is a bonus. * Knowledge of dimensional measurements, machining processes, millwork, welding, and materials handling enhances your suitability for this role. * Strong attention to detail with excellent hand-eye coordination for precise fabrication tasks. * Ability to work both independently and as part of a team in fast-paced settings while maintaining safety standards. Join us in creating exceptional stone surfaces that stand the test of time! We value energetic individuals eager to develop their skills in a supportive environment dedicated to quality craftsmanship and safety excellence. All positions are paid roles committed to your professional growth within our vibrant team! Pay: From $23.00 per hour Work Location: In person
General Atomics (GA), and its affiliated companies, is one of the world’s leading resources for high-technology systems development ranging from the nuclear fuel cycle to remotely piloted aircraft, airborne sensors, and advanced electric, electronic, wireless and laser technologies. General Atomics Electromagnetic Systems (GA-EMS) designs and manufactures first-of-a-kind electromagnetic and electric power generation systems. GA-EMS’ expanding portfolio of specialized products and integrated system solutions support critical fleet, space systems and satellites, missile defense, power and energy, and process and monitoring applications for defense, industrial, and commercial customers worldwide. We have an exciting opportunity for an Electromagnetic Aircraft Launch System (EMALS) and Advanced Arresting Gear (AAG) Production Project Manager to join our team located in Rancho Bernardo, CA. The Production Project Manager plays a critical role in meeting financial business objectives and delivering hardware and contractual documentation for the EMALS and AAG systems. This position is responsible for overseeing and coordinating the operational aspects of one or more production project(s) that may involve hardware, firmware, and/or software, and teams of 10-75 project members. DUTIES & RESPONSIBILTIES: Deliver EMALS and AAG hardware and documentation per contract requirements and business objectives. Provide leadership, direction, and guidance to employees working on assigned projects. Effectively communicate project expectations and assign tasks/priorities to team members and stakeholders in a timely fashion. Assign and monitor work of project management staff, providing technical support and direction when necessary. Create project plan(s) and manage resources to ensure project schedule, budget, quality, and specification goals are attained. Oversee and monitor project schedule, timelines, and milestones to meet delivery goals. Assess project issues and develop solutions to meet production, quality, and customer-satisfaction goals and objectives. Responsible for decisions which have an impact on outcomes and where failure to complete assignments will typically result in serious delays and expenditure of additional resources. Develop and deliver progress reports, proposals, requirements documentation, and presentations. Develop mechanisms for monitoring project progress and problem solving with project management, line management, and the customer. Interpret and administer policies, processes and procedures that impact project(s). Collaborate across management and project team to expand services and potential business opportunities. May participate in, lead segments of, or provide overall management for the request for proposal (RFP) process to generate new business. Maintain the strict confidentiality of sensitive information. Responsible for ensuring all laws, regulations and other applicable obligations are observed wherever and whenever business is conducted on behalf of the Company. Responsible for ensuring work is accomplished in a safe manner in accordance with established operating procedures and practices. Other duties as assigned or required. We recognize and appreciate the value and contributions of individuals with diverse backgrounds and experiences and welcome all qualified individuals to apply. Job Qualifications Typically requires a Bachelors or Masters in manufacturing, engineering, or related technical field and eleven or more years of progressively complex experience in the project administration experience with at least five of those years in project management. May substitute equivalent experience in lieu of education. Experience with Government contracts, lean manufacturing process, quality documentation, and/or Cost Account Management is highly desired. Must demonstrate an extensive understanding of project management processes and procedures, planning and scheduling methods, and budget management as well as the ability to organize, schedule, and coordinate workloads to meet established milestones and budgets. Must possess: The ability to initiate, plan, and manage simultaneous projects; The ability to identify issues, analyze and interpret data and develop solutions to a variety of non-routine matters of diverse scope and nature; Strong communication, leadership, presentation, and interpersonal skills are required to enable an effective interface with other departments, all levels of management, professional and support staff, customers, potential customers, and government representatives; Must be proficient at managing teams to ensure all activities are completed on time and within budget; Hands-on experience with Earned Value Management System requirements and metrics is required; Customer focused, must be able to work on a self-initiated basis and in a team environment, and able to work extended hours and travel as required. Must hold or be able to attain a Secret clearance for potential cybersecurity requirements. Job Category Program/Project Management Experience Level Senior (8+ years) Workstyle Onsite Full-Time/Part-Time Full-Time Salary Pay Range Low 100,290 Pay Range High 183,098 Travel Percentage Required 0% - 25% Relocation Assistance Provided? No US Citizenship Required? Yes Clearance Required? Desired Clearance Level Secret Search Jobs at | General Atomics and Affiliated Companies
AleSmith Brewing Company is dedicated to creating the world’s highest quality beer, while promoting an understanding and appreciation of craft beer and its styles and traditions to those we faithfully call our customers. *Job purpose* Under the general direction of the Brewery Manager, the *Brewer* _*(Morning shift 5am-1:30pm)*_ will be responsible for following Company safety procedures, policies, and SOPs (Standard Operating Procedures) to produce high quality beer to Company standards. Responsible for helping to keep brewery and equipment clean and sanitized. Will also assist in repair of and preventative maintenance of brewery equipment. *Duties and responsibilities* Include the following. Other duties may be assigned. * Perform brewing and cellar operations at the brewery, including day-to-day process issues, recipe management, operating policies, procedures, release parameters, and safety policies. * Ensure the cleanliness and sterilization of tanks, screens, inflow pipes, production areas, and equipment, using hoses, brushes, scrapers, or chemical solutions. * Responsible for following comprehensive Standard Operating Procedures with full documentation for brewing and cellar operations including raw material handling, wort production, fermentation, dry hopping, yeast handling, liquid transfer, fining, colloidal stabilization, separation, and carbonation. * Maintain detailed records of raw materials, quality checks and production stage timings. * Maintain accurate records. * Participate in continuing education related to brewing, brewery operations, and safety and regulatory requirements. * Report functionality and maintenance of brewing equipment, CIP equipment, water delivery equipment, and sewer related systems to management. * Perform other duties as assigned *Qualifications* To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. * Good verbal and written communication skills are required. * Must be available to work any shift in a 24-hour schedule including occasional holidays and weekends. * Must be at least 21 years of age. *Education and/or Experience* High school diploma or general education degree (GED). Brewing education and/or equivalent work experience preferred. AleSmith Brewing Company provides equal employment opportunities to all employees and applicants for employment regardless of race, color, religion, gender, sexual orientation, gender identity or expression, national origin, ancestry, age, genetic information, marital status, pregnancy, medical condition, physical disability, mental disability, veteran status or any other characteristic protected by state or federal law. Job Type: Full-time Pay: $19.00 - $24.00 per hour Benefits: * 401(k) * 401(k) matching * Dental insurance * Employee assistance program * Employee discount * Health insurance * Life insurance * Paid time off * Referral program * Vision insurance Work Location: In person
AleSmith Brewing Company is dedicated to creating the world’s highest quality beer while promoting an understanding and appreciation of craft beer and its styles and traditions to those we faithfully call our customers. We operate at the highest level of integrity and display excellence in all we do, from brewing to collaborating with each other and the organizations of our craft, and most of all, to the way we treat our customers. Job purpose The *Packaging Assistant* will assist in all packaging operations, including cleaning, maintaining all Packaging equipment, and keeping warehouses and supplies organized. Also, to assist with regular brewery and packaging equipment maintenance while following safety procedures and Company SOP’s (Standard Operating Procedures). Duties and responsibilities Include the following. Other duties may be assigned. * Assists with setup, cleaning, and operation of packaging machinery * Places packages in boxes, applies carriers, and stacks finished product * Operates forklift to move pallets around warehouse * Assists with conducting inventory and related documentation * Operates keg washing machine to wash and sanitize kegs * Assists in the troubleshooting, repair and preventative maintenance of brewery equipment * Performs general cleaning duties, such as cleaning floors, drains, packaging equipment, and all packaging areas * Assist in the transition of duties and communication between shifts * Participate in continuing education related to brewery and packaging operations, and safety and regulatory requirements * Assist in resolving customer issues and ensure customer satisfaction while maintaining the integrity of the Company * Follows all safety procedures and SOP’s and wear safety, personal protective equipment (PPE) Qualifications To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. * Must be at least 21 years of age * Ability to work some evenings, nights, weekends, and holidays * Proficiency in communication, including verbal and written skills * Ability to work with hazardous cleaning chemicals * Ability to routinely lift, push and pull 55 lbs * Ability to stand and walk for up to 10 hours a day * Be motivated, hard-working, safety-minded and innovative with a commitment to representing and enjoying the culture and success of AleSmith * Be an exceptional team player with the ability to work independently as well * Ability to stay organized and follow checklists, departmental guidelines and SOP’s AleSmith Brewing Company provides equal employment opportunities to all employees and applicants for employment regardless of race, color, religion, gender, sexual orientation, gender identity or expression, national origin, ancestry, age, genetic information, marital status, pregnancy, medical condition, physical disability, mental disability, veteran status or any other characteristic protected by state or federal law. Job Type: Full-time Pay: $19.00 per hour Benefits: * 401(k) * 401(k) matching * Dental insurance * Employee assistance program * Employee discount * Health insurance * Life insurance * Paid time off * Referral program * Retirement plan * Vision insurance Work Location: In person
*Accounts Payable (AP) Processor – Manufacturing* We are seeking a detail-oriented Accounts Payable Processor with experience in a manufacturing environment and strong QuickBooks skills. This role is responsible for managing the full cycle of accounts payable, ensuring accurate and timely processing of invoices, and maintaining vendor relationships. *Responsibilities: * * Process high-volume vendor invoices accurately * Perform 3-way matching (PO, receipt, invoice) * Verify pricing, quantities, and terms * Enter and manage invoices in QuickBooks * Process payments (checks, ACH, wires) * Reconcile vendor statements and resolve discrepancies * Maintain organized records and documentation * Assist with month-end close and reporting *Qualifications:* * 2+ years accounts payable experience * 2+ years QuickBooks experience * Manufacturing experience required * Strong Excel skills * High attention to detail * Ability to multitask in a fast-paced environment *Benefits: * * Competitive salary * Health, dental, and vision insurance * Paid time off * Growth opportunities Pay: $22.00 - $25.00 per hour Benefits: * Dental insurance * Health insurance * Paid time off Work Location: In person
At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient’s mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds. As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels included, respected, empowered and recognised. What You Can Expect The senior manufacturing engineer is responsible for providing manufacturing engineering services to support efficient manufacturing processes. Engineering services may include cell management, process development, project management, process validation, tool design, and trouble shooting. How You'll Create Impact Creating, maintaining, and improving controlled technical documents such as prints, procedures, bill of materials and routers. Supporting a wide variety of processing applications such as machining, finishing, forging, casting, cleaning, heat treating, bonding, molding, etc. Conducting feasibility study to estimate product cost and analyze capital equipment, capacity, and capability requirements Establishing and improving process methods which meet performance and quality requirements Developing and executing project plans and schedules for work activities Communicate (written and verbal) direction and project plans with appropriate personnel from other departments. Evaluating multiple options to select the most appropriate processes and machining methods Execute equipment qualification or process validation project(s) This is not an exhaustive list of duties or functions and might not necessarily comprise all of the essential functions for purposes of the Americans with Disabilities Act What Makes You Stand Out Skilled and knowledgeable in manufacturing and new product processing Competence with drafting standards and geometric dimensioning and tolerancing Ability to balance marketing, manufacturing, and design requirements to meet customer requirements Ability to lead and prioritize multiple medium complexity project assignments and complete work in a timely manner Good problem-solving skills through the use of quality and statistical tools Ability to effectively work within a cross-functional team to complete critical project tasks Demonstrates good written and verbal communication skills F-01694A Experienced with control procedures, such as the Change Management System, Nonconformance Reports, Engineering Specifications, Corrective and Preventive Action (CAPA), and Work Instructions Proficient with Statistical Process Control concepts, process development, CNC programming terminology, and tooling design concepts Microsoft Office Suite and Project Creating, maintaining, and improving controlled technical documents such as prints, procedures, bill of materials and routers. Supporting a wide variety of processing applications such as machining, finishing, forging, casting, cleaning, heat treating, bonding, molding, etc. Support deployment of Operational Excellence/Process improvement initiatives in the plant. Examples of these programs and initiatives are Cost Saving Program, Class A, Workflow Lean Transformation, Quality Begins with Me, DMAIC Problem Solving, Lean Six Sigma, Total Productive Maintenance, etc. Assists site leadership team in selecting and prioritizing projects that align with plant goals and strategies. Responsible for the sustaining and execution of cost saving program, metric tracking and reports within the site. Responsible to manage and complete Six Sigma Green Belt projects. Maintain Class A roadmap and timeline to incorporate into the overall Operational Excellence Strategy. Conducting feasibility study to estimate product cost and analyze capital equipment, capacity, and capability requirements. Establishing and improving process methods which meet performance and quality requirements. Developing and executing project plans and schedules for work activities Lead engineers as Project lead on Process improvement initiatives. Communicate (written and verbal) direction and project plans with appropriate personnel from other departments. Evaluating multiple options to select the most appropriate processes and machining methods. Execute equipment qualification or process validation project(s) Your Background B.S. in Engineering with a minimum of 3-5 years of manufacturing engineering experience. Knowledge in Lean Principles and or Six Sigma or other problem-solving methodology is preferred. Travel Expectations Up to 10% EOE/M/F/Vet/Disability
Valspec—a global provider of system validation and lifecycle services—provides commissioning and qualification of computerized systems for clients in the Life Sciences industry. Established in 1999, Valspec's mission is to provide a wide spectrum of services that help its clients meet their capital project and lifecycle maintenance goals. Valspec's projects are critical to the industry, and to the people who rely on its products. Many projects ensure that life-changing drugs are available to those who need them; others streamline production to meet demand at a lower cost, allowing for the discovery of new and innovative therapies. Validation Engineer (CQV) Location: Raleigh-Durham area, NC Position Overview We are seeking an experienced Validation Engineer (CQV) to support commissioning, qualification, and startup activities for a large-scale biopharmaceutical manufacturing facility. This role will focus on downstream process systems and requires strong hands-on field execution, system troubleshooting, and automation verification experience in a GMP-regulated environment. Key Responsibilities Perform field verification of P&IDs, equipment datasheets, vendor drawings, isometrics, and utility connections to confirm system accuracy and readiness ahead of commissioning and startup. Lead and execute mechanical completion walkdowns and turnover package (TOP) reviews, ensuring construction quality, punch list closure, calibration records, weld documentation, and redline updates are complete. Support commissioning readiness by validating system boundaries, flow paths, and equipment installation in alignment with design documentation. Execute commissioning and qualification (CQV) activities for downstream process equipment including: Chromatography skids Ultrafiltration/Diafiltration (UF/DF) systems Viral filtration systems Depth filtration units Buffer preparation vessels Product hold tanks Perform field startup and functional testing of chromatography systems, including: Flow path verification Valve sequencing checks Conductivity and pressure monitoring Automation functionality validation Conduct Operational Qualification (OQ) testing for automated systems using DeltaV, including: Loop checks and I/O verification Interlock and permissive testing Alarm challenge testing Control logic and sequence verification under live conditions Verify process alarms, interlocks, permissives, and emergency shutdown functions through field execution and control system testing. Perform detailed P&ID walkdowns and field verification of valves, instruments, and process flow to support system turnover, TOP approval, and final acceptance. Identify and troubleshoot startup issues related to: Automation logic and control sequences Valve sequencing and flow path discrepancies Equipment integration and skid interfaces Cleaning cycle performance Collaborate cross-functionally with engineering, construction, and operations teams to maintain project timelines and ensure successful system startup. Required Qualifications Bachelor's degree in Engineering (Chemical, Mechanical, or related discipline) or equivalent industry experience 5+ years of experience in CQV, commissioning, or validation within biopharmaceutical or life sciences manufacturing Hands-on experience with downstream processing equipment, especially chromatography and filtration systems Strong knowledge of cGMP requirements, commissioning processes, and validation lifecycle Experience executing OQ protocols and field testing activities Familiarity with DeltaV or similar DCS platforms (Emerson experience preferred) Proficiency in reading and interpreting P&IDs, isometrics, and technical drawings Demonstrated ability to work in a fast-paced startup environment with significant field presence Preferred Qualifications Previous experience supporting greenfield or large-scale capital projects Strong troubleshooting and problem-solving skills in live plant environments Experience with automation systems integration and process control verification Ability to manage multiple systems and priorities during commissioning/startup phases Work Environment Primarily field-based role with significant time in manufacturing and construction areas Requires coordination with multiple stakeholders across CQV, engineering, and operations May involve extended hours during critical commissioning and startup windows Why Join Valspec? At Valspec, we offer more than just a job — we provide a career experience rooted in a standout culture, collaborative environment, and a strong sense of ownership. Join a team where your contributions matter, your development is prioritized, and your success is shared. Why Join Valspec? At Valspec, we offer more than just a job — we provide a career experience rooted in a standout culture, collaborative environment, and a strong sense of ownership. As an Employee Stock Ownership Plan (ESOP) company, every team member has a stake in our success, fostering a shared commitment to excellence and innovation. We also offer a highly competitive benefits package, including: Premium medical coverage 401(k) with company match Tuition reimbursement Unique performance incentives And more — all designed to support your growth, well-being, and future. Join a team where your contributions matter, your development is prioritized, and your success is shared. When receiving e-mails from a Proconex or Valspec recruiter, you will only receive e-mails from addresses ending in @proconexdirect.com, @proconex.net or @valspec.net. Any other domains are impersonations and should be ignored. Candidates must be legally eligible to work in the United States without company sponsorship. Also, we are not interested in working on a corp-to-corp basis with other companies at this time. Any third-party unsolicited resume submission(s) will immediately become the property of Valspec. Valspec will not pay any fee to a submitting employment agency, person, or entity unless a signed agreement is established. Valspec is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to sex, race, color, religion, national origin, age, sexual orientation, gender identity, disability, protected veteran status or any other protected class. We are committed to providing a professional environment free of any discrimination or harassment, and we are proud to be a Drug-Free Workplace.
Sewing Machine Operator Sunset West, a division of Hooker Furnishings Corporation, is currently recruiting Sewing Machine Operators. Sunset West specializes in luxury outdoor furniture for residential and hospitality markets. Hooker Furnishings, celebrating over a century in business, is a designer, marketer, and importer of case goods, leather, fabric-upholstered, and outdoor furniture. We are looking for a dependable individual with great attention to detail to join our sewing team. Main duties include, but are not limited to: Operate industrial sewing machine to join cut fabric parts to fabricate upholstery coverings Sort the fabric and pieces Read and understand work ticket for identifying order details Candidates that will be a great fit will: Have previous sewing experience Be able to work seated 8 hours a day and work independently Have a strong attention to detail and desire to sew not just quantity, but high quality Why should you apply? · A company committed to DEI (Diversity, Equity, and Inclusion) values · Competitive compensation and incentive plan · Competitive PTO plan · 8 paid holidays and 2 floating holidays. · Comprehensive medical, dental, vision plans including a generous employer health saving account (HSA) contribution each plan year · Matching 401k employer contributions · A caring, family-focused culture Shift: Monday-Friday 8-hour shift. Overtime opportunities available. Pay: Starting wage $19 plus incentive pay Hooker Furnishings Corporation provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
What if the work you did every day could impact the lives of people you know? Or all of humanity? At Illumina, we are expanding access to genomic technology to realize health equity for billions of people around the world. Our efforts enable life-changing discoveries that are transforming human health through the early detection and diagnosis of diseases and new treatment options for patients. Working at Illumina means being part of something bigger than yourself. Every person, in every role, has the opportunity to make a difference. Surrounded by extraordinary people, inspiring leaders, and world changing projects, you will do more and become more than you ever thought possible. Seeking a highly motivated and team-oriented Manufacturing Chemist with experience in organic synthesis to join our Nucleotide Manufacturing group. Manufacture and test components and reagents of moderate to high complexity in a quality manner on standard laboratory equipment by following work instructions and test methods. The candidate must have a strong understanding of purification and analytical techniques used in the manufacture of complex nucleotides and/or oligonucleotides, such as Ion Exchange and Reverse Phase Chromatography. The candidate should have 0- 2 years of chemistry bench experience in synthetic processes. Position Responsibilities: Follow all SOP's and WI's as required by the Quality Management System Plan and execute daily work with occasional supervision Assemble data for analysis using accepted methods Assess results of work and compare data against identifiable factors. Summarize work accurately. Determine appropriate action(s) by exercising judgement within defined procedures and practices. Follow all safety rules at Illumina and apply all relevant protocols to work responsibilities Executes simple experiments (troubleshooting, OOE, OOS, etc) designed by senior lab personnel Identify non-conformances in work Use basic Operational Excellence tools to identify root cause of problems Completes ERP and MES transactions for manufacturing work order processing Synthesizes molecules using industry standard instrumentation and techniques. May perform purification of synthesized molecules, while monitoring performance through analysis of chromatograms. May collect, prepare, and analyze product fractions using analytical HPLC techniques to determine product quality. Measures and adjusts product concentration or mix by using applicable instrumentation. Formulates buffers required for processing and storing target molecules throughout production. Listed responsibilities are an essential, but not exhaustive list, of the usual duties associated with the position. Changes to individual responsibilities may occur due to business needs. Position Requirements: 0-2 years of experience in synthetic chemistry processes, purification, and QC analysis of organic molecules. Familiarity with standard laboratory equipment (HPLCs/UPLCs, synthesizers, reactors, rotary evaporators, UV/Vis spectrophotometers, pH meters, etc) Solid technical knowledge of synthetic organic chemistry, HPLC methods, manufacturing processes, and manufacturing execution systems. Ability to work with ERP, EAM, MES, and Quality systems (SAP, Camstar, Teamcenter, etc) Excellent written and verbal communication skills required. Basic understanding of equipment/instrument upkeep, calibration, and maintenance policies. Ability to carry up to 40 lbs All listed requirements are deemed as essential functions to this position; however, business conditions may require reasonable accommodations for additional task and responsibilities. Preferred Experience/Education/Skills: Typically requires a Bachelor’s degree and a minimum of 0-2 years of related experience; or equivalent work experience. The estimated base hourly range for the Manufacturing Chemist 1 role based in the United States of America is: $27.50 - $41.25. Should the level or location of the role change during the hiring process, the applicable base pay range may be updated accordingly. The range reflects long‑term growth in the role; therefore, most candidates are hired between the minimum and middle of the range. Placement depends on experience, skills, location, and internal equity. Additionally, all employees are eligible for one of our variable cash programs (bonus or commission) and eligible roles may receive equity as part of the compensation package. We offer a wide range of benefits as innovative as our work, including access to genomics sequencing, family planning, health/dental/vision, retirement benefits, and paid time off. We are a company deeply rooted in belonging, promoting an inclusive environment where employees feel valued and empowered to contribute to our mission. Built on a strong foundation, Illumina has always prioritized openness, collaboration, and seeking alternative perspectives to propel innovation in genomics. We are proud to confirm a zero-net gap in pay, regardless of gender, ethnicity, or race. We also have several Employee Resource Groups (ERG) that deliver career development experiences, increase cultural awareness, and offer opportunities to engage in social responsibility. We are proud to be an equal opportunity employer committed to providing employment opportunity regardless of sex, race, creed, color, gender, religion, marital status, domestic partner status, age, national origin or ancestry, physical or mental disability, medical condition, sexual orientation, pregnancy, military or veteran status, citizenship status, and genetic information. Illumina conducts background checks on applicants for whom a conditional offer of employment has been made. Qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable local, state, and federal laws. Background check results may potentially result in the withdrawal of a conditional offer of employment. The background check process and any decisions made as a result shall be made in accordance with all applicable local, state, and federal laws. Illumina prohibits the use of generative artificial intelligence (AI) in the application and interview process. If you require accommodation to complete the application or interview process, please contact [email protected]. To learn more, visit: https://www.dol.gov/ofccp/regs/compliance/posters/pdf/eeopost.pdf. The position will be posted until a final candidate is selected or the requisition has a sufficient number of qualified applicants. This role is not eligible for visa sponsorship.
JOB DESCRIPTION Jubilant Radiopharmacies is proud to becertified as a Great Place to Work®, recognizing our commitment to a respectful, supportive, and people-first culture. As aPET Manufacturing Technician, you will play an important behind-the-scenes role in healthcare. Your work helps doctors diagnose disease and care for patients every day. This is a hands-on opportunity to work in a healthcare manufacturing environment, learn specialized equipment, and build a meaningful career — no college degree required. You will be trained to safely operate equipment, follow clear procedures, and support the production and quality testing of PET radiopharmaceuticals. The work shift for this position will be 2:00am - 10:00am Key Responsibilities Prepare equipment and work areas for daily production following written procedures Operate cyclotron and chemistry equipment using computer-based controls Produce PET radiopharmaceuticals that support patient diagnosis and care Perform quality checks to ensure products meet safety and regulatory standards Clean and maintain equipment and workspaces Prepare products for shipment, including labeling and required documentation Monitor supplies and notify leadership when materials are needed Follow all safety, quality, and compliance requirements at all times Work as part of a team to meet daily production schedules Participate in training and ongoing learning Qualifications High School Diploma or equivalent Willingness to learn and follow detailed procedures Strong attention to detail and safety Ability to work well as part of a team Basic computer skills Clear verbal and written communication skills Prior experience in manufacturing or healthcare is helpful but not required Must be able to pass a background check and pre-employment drug test (USA only) Valid driver’s license required (USA only) All regulatory, safety, and compliance requirements must be followed exactly as trained and documented. Physical Requirements Ability to occasionally lift items up to 65 lbs Ability to perform work requiring focus, accuracy, and visual attention Benefits We offer competitive compensation, generous vacation, and 401K matching. Equal Employment Opportunity Statement Jubilant Radiopharmacies is an equal opportunity employer. We are committed to building a diverse and inclusive workplace where all employees feel valued and supported. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other legally protected status.