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San Diego, CAManufacturing – Manufacturing /Full Time /On-Site With extensive experience in developing biologics and bioconjugates, we offer a seamless service delivered by fully integrated teams, from early discovery to commercial manufacturing. Forward-thinking and committed, we find the best solution and use the right technologies to design, develop and manufacture your products to ensure we get vital medicines to patients quickly and safely. We are dedicated to quality excellence. We are driven to get better treatments to market, efficiently and responsibly by reducing timelines and delivering the highest quality products and services. We are Abzena. More than a CDMO, we are a responsible and dedicated partner that takes care of your products from concept to patient. The Senior Manufacturing Specialist is a technical subject matter expert supporting late-stage clinical and commercial biologics production. This role is responsible for leading and supporting manufacturing investigations, identifying true root causes, and developing effective corrective and preventative actions (CAPAs). The Senior Manufacturing Specialist will also play a key role in driving process improvement initiatives to ensure compliance, efficiency, and operational excellence. The ideal candidate will bring strong cGMP manufacturing experience along with exceptional written and verbal communication skills to collaborate effectively across Manufacturing, Quality, Development, and other functions. Responsibilities Serve as SME for manufacturing operations, equipment, and processes. Lead investigations into deviations, process failures, and equipment issues, ensuring accurate root cause identification and timely resolution. Author clear, concise, and technically sound investigation reports and CAPA documentation. Develop and implement effective CAPAs that address underlying issues and ensure sustainability. Drive continuous improvement initiatives to optimize manufacturing processes, increase efficiency, and strengthen compliance. Partner with cross-functional teams (Quality, Development, Engineering, Supply Chain) to ensure alignment on solutions and process changes. Provide technical expertise and support during regulatory inspections, audits, and internal reviews. Analyze production data and KPIs to identify trends, risks, and opportunities for improvement. Mentor and support operations staff in applying root cause analysis and problem-solving tools. Qualifications Bachelor’s degree in Engineering, Life Sciences, or related discipline; advanced degree preferred. Minimum 3 years of hands-on experience in a cGMP manufacturing environment, with strong preference for late-stage clinical or commercial biologics. Demonstrated expertise in root cause analysis methodologies (e.g., 5-Whys, Fishbone, FMEA). Proven ability to develop and implement effective CAPAs and sustainable process improvements. Strong technical writing skills and excellent verbal communication skills. Ability to clearly present technical findings to diverse audiences, including cross-functional teams and regulatory inspectors. Strong organizational skills and ability to manage multiple priorities in a fast-paced environment. Physical Requirements Ability to stand for 1-2 hours at a time, sit for 2 to 3 hours at a time. Frequently lift and or move objects up to 30 pounds. Stand/walk during entire length of shift. Use arms, hands and fingers to handle, feel or reach. Ability to climb, balance, stoop, kneel, crouch, or crawl. Visual abilities including near and far sight, color, peripheral vision, depth and ability to focus. $90,000 - $120,000 a year FLSA: Exempt Abzena is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws. This policy applies to all employment practices within our organization, including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, and training.
THE POSITION Who we are A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche. Genentech is the founder of the biotechnology industry and has been delivering on the promise of biotechnology for more than 43 years. It has been a member of the Roche Group since 2009 and is one of its most important centres of pharmaceutical research. At Roche, the patient is at the heart of all R&D efforts, and delivering life-changing therapies to patients while also driving positive change in the global society is the impetus to everything we do. The Opportunity As a Manufacturing Technician, you will work within a team to produce and deliver quality products for patients around the world. We are a 24/7 site and the work load is divided across multiple organizations. Technicians are expected to work in a safe manner and follow our Standard Operating Procedures at all times. Doing these two critical aspects of our job helps us maintain our right to operate and commitment to governing bodies around the world. Our Manufacturing begins in Upstream Cell Culture, where we thaw and scale up our process. Some of the responsibilities include preparing the medium needed for cell growth, monitoring cell cultures, and assembly/disassembly of single use and/or stainless steel bioreactors. Subsequent to the cell culture phase is a series of operations to isolate, purify, and formulate the medicines. This includes activities such as preparation of buffers, cleaning and sterilization of equipment, operation of chromatography processes, and assembly and operation of single use equipment. Who you are: You are someone who wants to influence your own development and can work independently, with limited supervision. You are looking for a company where you have the opportunity to pursue your own interests; where a job title is not considered the final definition of who you are, but the starting point. Experience with biologics manufacturing is not necessary but preferred. Candidates must be able to work any of the following manufacturing shifts: - 12 hr Day Shift, 6:00 am – 7:00 pm, - Sunday -Tuesday plus every other Wednesday - Wednesday – Friday plus every other Saturday - 10 hr Day Shift, 6:00 am – 4:30 pm - Sunday - Wednesday - Wednesday - Saturday - 10 hr Swing Shift, 3:30 pm -2:00 am - Sunday - Wednesday - Wednesday - Saturday - 12 hr Night Shift, 6:00 pm -7:00 am - Sunday-Tuesday plus every other Saturday - Wednesday – Friday plus every other Saturday Onboarding practices vary with area, but may consist of a multi-week schedule of Monday - Friday 8am - 5pm followed by on the job training for multiple weeks Monday - Thursday or Tuesday - Friday 1:00pm - 11:30pm. Once onboarding and/or training is complete, you will be released to your assigned Manufacturing shift. Shift availability will be determined by matching candidates strengths to shift needs and are subject to change based on business needs and production schedules. Behaviors, competencies, and qualities of the ideal applicant: Hardworking and fast learning individual that thrives in a high paced environment Experience in clean room environment and familiarity with cGMP and ISO/FDA standards is strongly preferred Ability to think critically and work both tactically and strategically Strong quality mindset with attention to detail and a desire to deliver service excellence Ability to work effectively with others, exhibiting a professional manner and establish constructive working relationships Qualifications / Requirements: Proficiency in the English language- reading, writing, and communication. Must be able to work all shifts, required overtime as needed, and stand for extended periods of time. Must be able to interface with computer systems to successfully operate manufacturing equipment. Experience with distributed control systems or other manufacturing automation is preferred. Must be able to successfully pass all job-related tests and certifications required for working in a cGMP quality environment including but not limited to: inspections and GMP requirements to perform essential functions of the job. Must re-qualify every year on all job-related training and certifications as job or qualifications require. May climb upwards of 6 flights of stairs a day to maneuver within the manufacturing facility. Lifting up to 25lbs may be required. The cleanroom environment requires that company provided gowning is worn. This may include plant uniform, coveralls, gloves and safety shoes. Additionally, regulations prohibit makeup, jewelry, and other personal items from entering the clean room environment. Education / Experience / Attributes (By Level): Scientific and technical degrees preferred, e.g. Life Science or Engineering Experience in a GMP working environment with Background in Cell Culture/Purification is highly desired with experience in the operation of complex mechanical equipment used in the washing, autoclaving, processing, and assembly of parts used in Upstream or Downstream processes Target industries include pharmaceutical, biotechnology, biomedical, electronic, and chemical, food, cosmetics, and/or other medical industries. Understands the theory, concepts, and regulations behind biopharma technology and processes. - Manufacturing Technician (MT2) Bachelor degree with 1 year related experience, or Associate degree with 3 years experience, or High school with 5 years experience Biotech certificate from approved program is considered a plus Ability to receive, interpret and provide basic information and materials involved with the day to day activities of performing the job The expected salary range for this position based on the primary location of Oceanside is $42,400 - $78,800. - Senior Manufacturing Technician (MT3) Bachelor degree with 3 years experience, or Associate degree with 5 years experience, or High School with 7 years experience Biotech certificate from approved program is considered a plus Capable of writing detailed reports and summaries Must possess a high level of automation and technical process knowledge as related to prep and process within area of responsibility The expected salary range for this position based on the primary location of Oceanside is $51.000 - $94,800. Relocation benefits are not available for this job posting. This position also qualifies for the benefits detailed at the link provided below. Benefits Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws. If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants. JOB FACTS Job Sub Category Manufacturing Schedule Full time Job Type Regular Posted Date Sep 22nd 2025 Job ID 202505-111769
Position Summary To safely and effectively run equipment related to HPP/Bottling/Packaging and Pack Out. Operator 2 will demonstrate the ability to run all machines within one department e.g. All machines associated with the Bottling department. Schedule Wednesday-Sunday, 5AM - 1:30 PM Essential Duties and Responsibilities Including but not limited to: To run all machines safely and effectively within your department including but not limited to: Fillers, HPP’s, Labelers, Case Packers, Bundlers, Sleevers, Palletizers, etc. Plan to ensure you have the correct materials, equipment, and ingredients for each day. Communicate with your Shift Lead/Supervisor/Manager to advise of any issues/concerns. Communicate well with other employees. Follow all OSHA rules regarding safe machine operation. Keep your work area clean, organized, and safe always. Keep your work area clean, organized, and safe always Adhere to SOP, SSOP, GMP, and HACCP guidelines when in the plant. Department Machine Bottling Depal GRX Unscrambler F4 F5 Shot Filler Carbonated Filler HPP HPP 1 - 2 HPP 3 - 4 Trines Sleever Packaging/Pack Out Bundlers (Dimac, KHS, SMI) Drop Packer Unscrambler Job Qualifications Experience: Preferred 3+ years’ experience working in a manufacturing/warehouse environment Other Skills: Must have strong leadership skills. Problem solver skills Other Abilities: Be able to work independently with moderate supervision Ability to think ahead. Responsibilities may require an adjusted work schedule, overtime, evening/weekend hours in order to meet deadlines. Working & Environmental Conditions You’ll work in diverse environments, including: A wet, refrigerated manufacturing facility (below 40°F) A dry warehouse (up to 85°F) Freezer storage areas (as low as –10°F) Work areas may be tight and loud, with continuous exposure to noise levels over 85 dBA. You'll be required to follow strict safety protocols and consistently wear personal protective equipment (PPE), including safety glasses, ear protection, and steel-toed shoes. The position involves repetitive tasks that must be performed safely and efficiently. Physical Demands To succeed in this role, you must be able to: Stand and walk throughout the entire shift Lift and carry up to 50 lbs continuously Push/pull up to 100 lbs with consistent motion Bend, kneel, twist, squat, and reach overhead with both arms Climb ladders and stairs, and work at heights when needed Use your hands frequently for gripping and handling materials Work near moving machinery Pass a pre-employment physical exam Why Join Suja? We’re proud to offer a competitive benefits package that supports your well-being, including: Medical, dental, vision, and life insurance Additional ancillary benefits 401(k) with company match Paid vacation, sick time, and holidays And of course, Juice Benefits! Compensation $18.00-19.00/HR #ZR #INDHP Suja Life is proud to be an equal opportunity employer seeking to create a welcoming and diverse environment. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, ancestry, physical or mental disability, medical condition, marital status, genetics, age, or veteran status or any other applicable legally protected status or characteristic. The Company complies with all federal/local/state regulations regarding pay. Equal Opportunity Employer This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.
With extensive experience in developing biologics and bioconjugates, we offer a seamless service delivered by fully integrated teams, from early discovery to commercial manufacturing. Forward-thinking and committed, we find the best solution and use the right technologies to design, develop and manufacture your products to ensure we get vital medicines to patients quickly and safely. We are dedicated to quality excellence. We are driven to get better treatments to market, efficiently and responsibly by reducing timelines and delivering the highest quality products and services. We are Abzena. More than a CDMO, we are a responsible and dedicated partner that takes care of your products from concept to patient. The Senior Manufacturing Specialist is a technical subject matter expert supporting late-stage clinical and commercial biologics production. This role is responsible for leading and supporting manufacturing investigations, identifying true root causes, and developing effective corrective and preventative actions (CAPAs). The Senior Manufacturing Specialist will also play a key role in driving process improvement initiatives to ensure compliance, efficiency, and operational excellence. The ideal candidate will bring strong cGMP manufacturing experience along with exceptional written and verbal communication skills to collaborate effectively across Manufacturing, Quality, Development, and other functions. Responsibilities Serve as SME for manufacturing operations, equipment, and processes. Lead investigations into deviations, process failures, and equipment issues, ensuring accurate root cause identification and timely resolution. Author clear, concise, and technically sound investigation reports and CAPA documentation. Develop and implement effective CAPAs that address underlying issues and ensure sustainability. Drive continuous improvement initiatives to optimize manufacturing processes, increase efficiency, and strengthen compliance. Partner with cross-functional teams (Quality, Development, Engineering, Supply Chain) to ensure alignment on solutions and process changes. Provide technical expertise and support during regulatory inspections, audits, and internal reviews. Analyze production data and KPIs to identify trends, risks, and opportunities for improvement. Mentor and support operations staff in applying root cause analysis and problem-solving tools. Qualifications Bachelor’s degree in Engineering, Life Sciences, or related discipline; advanced degree preferred. Minimum 3 years of hands-on experience in a cGMP manufacturing environment, with strong preference for late-stage clinical or commercial biologics. Demonstrated expertise in root cause analysis methodologies (e.g., 5-Whys, Fishbone, FMEA). Proven ability to develop and implement effective CAPAs and sustainable process improvements. Strong technical writing skills and excellent verbal communication skills. Ability to clearly present technical findings to diverse audiences, including cross-functional teams and regulatory inspectors. Strong organizational skills and ability to manage multiple priorities in a fast-paced environment. Physical Requirements Ability to stand for 1-2 hours at a time, sit for 2 to 3 hours at a time. Frequently lift and or move objects up to 30 pounds. Stand/walk during entire length of shift. Use arms, hands and fingers to handle, feel or reach. Ability to climb, balance, stoop, kneel, crouch, or crawl. Visual abilities including near and far sight, color, peripheral vision, depth and ability to focus. FLSA: Exempt Abzena is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws. This policy applies to all employment practices within our organization, including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, and training.
With extensive experience in developing biologics and bioconjugates, we offer a seamless service delivered by fully integrated teams, from early discovery to commercial manufacturing. Forward-thinking and committed, we find the best solution and use the right technologies to design, develop and manufacture your products to ensure we get vital medicines to patients quickly and safely. We are dedicated to quality excellence. We are driven to get better treatments to market, efficiently and responsibly by reducing timelines and delivering the highest quality products and services. We are Abzena. More than a CDMO, we are a responsible and dedicated partner that takes care of your products from concept to patient. The Quality Assurance Associate I/II, Quality Operations will ensure the site performs in a state of compliance by supporting Quality oversight activities and fostering an empowered culture of quality across manufacturing processes.The Associate will support on the floor activities, perform batch record review of buffer/medias/process records, support Deviations/ Change Controls / CAPAs and support quality workstreams as required. Responsibilities Provide hands-on QA collaboration and oversight to staff, ensuring compliance to good documentation practices, data integrity compliance, site inspection readiness SOPs, and relevant Good Regulated Practice (GxP) requirements. Work on the floor during production and help make quality decisions to ensure compliance with procedures and regulations. Perform Raw material sampling and release of utilities as and when needed by QA Raw Material team. Perform regular area walkthroughs of the manufacturing and Quality Control areas. Author minor deviations for topics that pertain to Quality Assurance Operations. Author Standard Operating Procedures (SOPs) for topics that pertain to Quality Assurance Operations. Perform batch record review for buffer / media, upstream and downstream manufacturing batch records. Perform disposition of buffer/media solutions manufactured at Abzena. Review and approve manufacturing deviations (minor), CAPAs, change controls and Standard Operating Procedures (SOPs). Support other departments as required to fulfill business needs. Comply with Abzena's policies and procedures. Communicate effectively with supervisors and colleagues. Participate effectively as a team player in all aspects of Abzena's business. Adhere to quality standards set by regulations and Abzena policies, procedures, and mission. Qualifications Minimum of B.S. degree in Life Sciences or Engineering with 2 years of experience in a GMP regulated Biopharmaceutical facility or equivalent. 1-3 years of experience in a Quality Assurance-related function. Experience overseeing manufacturing operations, batch record review and quality record. Knowledge of industry standards and regulation requirements for biologics and parenteral products in clinical development and commercial. Knowledge of GMP regulations (US, EU and ROW), good documentation practices, cGMP, 21CFR, USP and other applicable regulations, standards, and guidance. Ability to work in a cross-functional environment and resilience to a fast-paced environment. Physical Requirements Ability to stand for 3-4 hours at a time and sit for 2 to 3 hours at a time. Frequently lift and or move objects up to 30 pounds. Stand/walk during the entire length of shift. Use arms, hands, and fingers to handle, feel or reach. Ability to climb, balance, stoop, kneel, crouch, or crawl. Visual abilities including near and far sight, color, peripheral vision, depth, and ability to focus. Please note that this range encompasses both QA Associate I and II ranges FLSA: Non-Exempt Abzena is an equal-opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws. This policy applies to all employment practices within our organization, including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, and training.
Description FFP Company is currently seeking a Batching Operator to join our team. As a Batching Operator, you will be responsible for preparing, measuring, and mixing ingredients according to batch paperwork and recipes to create products with exceptional food protection, texture, color, and flavor. Including completion of quality checks, verification of rework being used. Responsibilities Accurately follow batch paperwork and recipes to prepare the products with the correct ingredients, weights, and measurements. Operate batching equipment such as scales, blenders, mixers, and pumps to process materials including SOPs. Monitor the equipment and process to ensure quality standards are met. Troubleshoot issues that arise during the batching process. Communicate effectively with the production team and shift supervisor. Maintain a clean and organized work area. Adhere to all safety, GMP, and quality regulations and procedures. Partner with Quality Assurance Technicians for product approvals and variances Work alongside Extraction and Packaging department to ensure product availability for efficient scheduling. Complete Clean-In-Place (CIP) as needed. Other duties as assigned. Requirements High school diploma or GED equivalent. Prior experience in food or beverage manufacturing, batching, or related field is preferred. Ability to read and interpret documents such as batch paperwork, recipe cards, and safety rules. Good math skills and ability to calculate weights and measurements. Basic computer skills. Strong attention to detail and ability to multi-task. Ability to work in a fast-paced environment and adhere to production schedules. A team player with good communication skills. Benefits Medical, Dental, Vision, and Prescription Drug Insurance effective on the first of the month following start date Health and Wellness Incentives 10 Days of Vacation 9 Paid Company Holidays 5 Personal Days 401(k) Health Savings Account (H.S.A.) Long-Term and Short-Term Disability Life Insurance Accidental Death & Dismemberment (AD&D) Employee Assistance Program (EAP)
Manufacturing Blending Operator Job Description Revised March 2021 Supervisor’s Title: Manufacturing Supervisor Department: Manufacturing Location: Carlsbad, CA Exempt Status: Non-Exempt Position Backed Up By: Manufacturing Supervisor Starting Pay: $21.12 At Glanbia Nutritionals Inc., our portfolio centers on dairy and non-dairy nutritional ingredients. We co-innovate and deliver ingredient solutions and precision premixes for use in the mainstream food and beverage, infant and clinical, and functional nutrition markets. We are the number one provider of whey-based nutritional ingredients globally and the number one producer of American-style cheddar cheese. Our protein systems have transformed the bar and beverage categories — bringing increased levels of protein, cleaner labels and greater product functionality to market. We have a direct presence in 21 countries, with manufacturing facilities in the US, Germany and China, and international sales and technical offices around the world. Job Summary Responsible for the preparation, production and packaging of blend material. Provides assistance to the operator and fills in for basic operator duties as assigned. Maintain blend equipment and production area cleanliness. Must complete all applicable SOP and QA trainings. Essential Functions Box Room duties - tape boxes, insert foil/plastic liners, apply labels to boxes Label bags, Zip tie liners, Tape filled boxes, Palletize boxes Hand clean separators, air flows, heat sealers, conveyors, scales, metal detectors Clean drains Prepare cell for wash - cover electronics, remove scan gun, apply appropriate LOTO Able to identify status of equipment and cell Operate hand jack and power jack (certified) Inspection of raw material and /or fill IBC Gather tools and supplies from tool room for blends or wash Operate conveyor metal detector, includes HACCP metal checks Basic Sampling / Aseptic Sampling Scale Check Scan in blends to NOAX Manufacturing and Inspection Cell Release Discharge blenders out of separator (not at line speed) Seal foil and plastic liners Able to assist the operator with all blending, milling, packing tasks Identify ingredient name, lot number and item number Operate High Pressure washer and Foamer Read and understand sequence of steps on BPR Screen, blend and package a variety of amino acids, vitamins and minerals, including those which are allergenic. Responsible for following the procedures for the preparation of blends and final blend product. Proper cleaning, blending, packaging and material inspection per Standard Operating Procedures. Proper cleaning of manufacturing equipment and production floor. Assist with routine maintenance on manufacturing equipment as requested by the Operator. Regular attendance is an essential function of this position. Following and living Glanbia values: Showing Respect, Winning Together, Finding a Better Way, Performance Matters, and Customers Champion. Each employee shall comply with occupational safety and health standards and all rules, regulations, and orders issued pursuant to the Occupational Safety and Health Act which are applicable to his/her own actions and conduct. Complies with all applicable food safety regulations and mandates Additional Functions Perform other duties as assigned Qualifications High School Diploma or GED preferred. Ability to work with amino acids, vitamins and fine chemicals in powder and liquid form as well as allergen products. Ability to follow direction and work with Standard Operating Procedures. Must be able to work flexible hours to include overtime and weekends on short notice Clear command of the English language both verbal and in writing. Basic computer knowledge. Typical Physical Activity Physical Demands The physical demands described represent those that must be met by an employee and the work environment characteristics are those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. · Regularly involves talking or listening, sitting, and the use of hands and fingers. · Regularly involves going up and down stairs. · Frequently involves reaching with hands and arms, standing and walking. · Occasionally involves crouching, stooping, kneeling and/or climbing or balancing. Physical Requirements Must be able to lift and carry items weighing up to 55 pounds. Manual dexterity sufficient to reach/handle items, works with the fingers, and perceives attributes of objects and materials. Involves moderate physical activity performing non-strenuous daily activities of a primarily administrative nature. Should be able to identify and distinguish colors, see clearly at 20 inches or closer and 20 feet or more, observe an area that can be seen up and down or to the left and right while eyes are fixed on a given point, judge distances and spatial relationships, and adjust the eye to bring an object into sharp focus. Typical Environmental Conditions May be exposed to moderate noise levels (i.e. office equipment, light traffic). May be exposed to moderate to high noise levels (i.e. production equipment, forklifts, heavy traffic). May be exposed to humidity, intense heat and cold, outdoor weather conditions, and fumes and toxic chemicals. May work in areas with mechanical moving parts, above ground with risk of fall, or areas with risk of electrical shock. Travel Requirements N/A Disclaimer Must perform the essential duties and responsibilities with or without reasonable accommodation efficiently and accurately without causing significant safety threat to self or others. The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and/or skills required of all personnel so classified. At Glanbia, we celebrate diversity, because we know that our individual strengths make us stronger together. We welcome and encourage interest from a wide variety of candidates, and we will give your application consideration, without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, or disability status. At Glanbia our culture will celebrate individuality, knowing that together we are more.
Dr. Bronner’s Company Culture Cool, kind, and capable employees are core to Dr. Bronner’s company culture! Our people are our greatest strength—strong and healthy relationships drive our success. Our workforce is impassioned, collaborative, engaged, and shares a commitment to diversity, inclusivity, and equity. Respect for differences in perspective and experience enriches our community with a sense of belonging. We seek to model a better, more just and caring world in how we show up for work, and how we show up for each other! “All-One!” Benefits As All-One, our employees are family. We support our employees to live their best life and to be happy and prosperous, with these benefits*: Full company-paid medical (PPO), dental, and vision for employees and dependents Annual discretionary bonus 13 paid holidays Profit-sharing plan for retirement Childcare assistance program Access to certain health services that may be limited in your state Dr. Bronner’s product discounts Education Investment Initiative Bring Your Dog to Work program Free daily vegan lunches Green Team and Toastmasters Vanpool Program Employee Giving Program *Please note that benefits are offered to eligible employees and are subject to specific terms and conditions. ______________________________________________________________________ Salary Range $89,000 - $95,000 depending on experience Location On-site position in Vista, CA. Schedule 1:00 PM to 10:00 PM Monday through Friday Responsibilities: Directs employees based on daily production needs. Assists with reviewing production orders for domestic customers and creating work schedules for production based on shipment schedules and confer with supporting department on work schedule. Ensures daily production requirements are achieved to meet customer expectations and works with leads and units to meet the demands of the department. Responsible for providing updates and support cross-departmentally related to inventory status, including the communication regarding international material with shipping and Ops Admin department to correctly reflect on ERP system. Plans, tracks, analyzes, and reports on projects/orders of varying contract type, size and complexity. Provides production/manufacturing work status reports for items such as change requests, new work item estimates, and resolution of potential schedule/work problems. Analyzes task/project schedule variances and advises management of discrepancies and anticipated problems in a timely manner. Prepares and maintains employee performance evaluations, corrective actions, performance development plans, trainings, time off requests, employee timecards and any employee related needs. Supports Production and lead manufacturing in identifying opportunities for improvements and optimization. Assists with assessing employee production needs, hiring, workflow, and termination of all assigned employees. Attends International Standards Organization (ISO), safety, production related meetings, management trainings. Assists with reviewing department budget reports and supporting with making best use of financial resources. Other duties as assigned within job scope. Qualifications: High school diploma or GED. 3-5 years of related experience with supervising and supporting a production/manufacturing team. At least 6 years in a manufacturing environment performing progressive experience in planning, budgeting, and performance measurements. Basic knowledge of Microsoft Office Programs (Word, PowerPoint, Excel, and Outlook.) We understand that not all candidates will meet every qualification and encourage all interested candidates to apply. Any combination of education and work experience that would be equivalent to the stated minimum requirements would qualify for consideration for this position. Dr. Bronner’s is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender identity or expression, sexual orientation, national origin, genetics, disability, age, marital status, sex (including pregnancy, childbirth, reproductive health decisions, breastfeeding, or related conditions), veteran status, or other basis protected by law.
San Diego, CAQuality – Quality Assurance /Full Time /On-Site With extensive experience in developing biologics and bioconjugates, we offer a seamless service delivered by fully integrated teams, from early discovery to commercial manufacturing. Forward-thinking and committed, we find the best solution and use the right technologies to design, develop and manufacture your products to ensure we get vital medicines to patients quickly and safely. We are dedicated to quality excellence. We are driven to get better treatments to market, efficiently and responsibly by reducing timelines and delivering the highest quality products and services. We are Abzena. More than a CDMO, we are a responsible and dedicated partner that takes care of your products from concept to patient. The Quality Assurance Associate I/II, Quality Operations will ensure the site performs in a state of compliance by supporting Quality oversight activities and fostering an empowered culture of quality across manufacturing processes.The Associate will support on the floor activities, perform batch record review of buffer/medias/process records, support Deviations/ Change Controls / CAPAs and support quality workstreams as required. Responsibilities Provide hands-on QA collaboration and oversight to staff, ensuring compliance to good documentation practices, data integrity compliance, site inspection readiness SOPs, and relevant Good Regulated Practice (GxP) requirements. Work on the floor during production and help make quality decisions to ensure compliance with procedures and regulations. Perform Raw material sampling and release of utilities as and when needed by QA Raw Material team. Perform regular area walkthroughs of the manufacturing and Quality Control areas. Author minor deviations for topics that pertain to Quality Assurance Operations. Author Standard Operating Procedures (SOPs) for topics that pertain to Quality Assurance Operations. Perform batch record review for buffer / media, upstream and downstream manufacturing batch records. Perform disposition of buffer/media solutions manufactured at Abzena. Review and approve manufacturing deviations (minor), CAPAs, change controls and Standard Operating Procedures (SOPs). Support other departments as required to fulfill business needs. Comply with Abzena's policies and procedures. Communicate effectively with supervisors and colleagues. Participate effectively as a team player in all aspects of Abzena's business. Adhere to quality standards set by regulations and Abzena policies, procedures, and mission. Qualifications Minimum of B.S. degree in Life Sciences or Engineering with 2 years of experience in a GMP regulated Biopharmaceutical facility or equivalent. 1-3 years of experience in a Quality Assurance-related function. Experience overseeing manufacturing operations, batch record review and quality record. Knowledge of industry standards and regulation requirements for biologics and parenteral products in clinical development and commercial. Knowledge of GMP regulations (US, EU and ROW), good documentation practices, cGMP, 21CFR, USP and other applicable regulations, standards, and guidance. Ability to work in a cross-functional environment and resilience to a fast-paced environment. Physical Requirements Ability to stand for 3-4 hours at a time and sit for 2 to 3 hours at a time. Frequently lift and or move objects up to 30 pounds. Stand/walk during the entire length of shift. Use arms, hands, and fingers to handle, feel or reach. Ability to climb, balance, stoop, kneel, crouch, or crawl. Visual abilities including near and far sight, color, peripheral vision, depth, and ability to focus. $60,000 - $80,000 a year Please note that this range encompasses both QA Associate I and II ranges FLSA: Non-Exempt Abzena is an equal-opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws. This policy applies to all employment practices within our organization, including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, and training.
We’re seeking experienced Cable Assemblers to join a high-performing team working on precision electronic and mechanical assemblies. This role involves tasks such as wiring, soldering, cable harnessing, and interpreting schematics and blueprints. *Responsibilities:* * Assemble cables, harnesses, and subassemblies using hand tools and schematics * Perform soldering and compression connections * Inspect and verify quality in accordance with control procedures * Disassemble, modify, and reassemble components as needed * Maintain a clean and safe work environment * Participate in training and continuous improvement activities *Qualifications:* * High school diploma or equivalent * Minimum 3+ years of experience in cable or electronic assembly * Ability to read schematics, blueprints, and wire lists * Familiarity with tools such as soldering irons, calipers, and tape measures * Ability to obtain a DOD security clearance * IPC620 certification and soldering certification preferred * Willingness to work overtime and flexible shifts * No C2C, C2H or similar candidates will be considered. *Apply Today!* If you’re detail-oriented, quality-driven, and ready to take on a hands-on role in a dynamic environment, we’d love to hear from you. Apply now! Job Types: Temp-to-hire, Contract Pay: $24.00 - $29.00 per hour Expected hours: No less than 40 per week Benefits: * 401(k) * Dental insurance * Health insurance * Vision insurance Application Question(s): * To be eligible for a DOD security clearance, candidates must pass a drug test and background check and be a U.S. citizen. Can you confirm that you meet these requirements? * Currently, no Corp to Corp, C2H, or similar candidates will be considered. Would that be a problem for you? Experience: * Long Haul Cable Assembly: 3 years (Preferred) License/Certification: * IPC-610 Certification (Preferred) Location: * Poway, CA 92064 (Preferred) Shift availability: * Day Shift (Preferred) * Night Shift (Preferred) Work Location: In person
Become part of a team that champions wellness worldwide. CAPTEK® Softgel International is a global leader in the development and production of high-quality nutraceutical supplements. As a contract manufacturer organization (CMO), we collaborate with innovators from some of the world’s most successful brands. We are actively hiring for 2nd Shift (2:00 PM - 10:15 PM)! Become part of a team that champions wellness worldwide. CAPTEK® Softgel International is a global leader in the development and production of high-quality nutraceutical supplements. Machine Operators • Technicians • Packaging • Inspection • Janitorial CAPTEK® is ACCEPTING APPLICATIONS for Production and Manufacturing positions. Responsibilities Include: • Operating equipment to defined standards and product requirement goals • Supporting a safe working environment by adhering to all plant safety, policies and procedures, including wearing appropriate Preventative Protective Equipment (PPE) • Conducting required quality checks on products to ensure customer satisfaction • Extensive amounts of reading, writing, and documenting • Working up to 8 hours per day in a loud/noisy, powdery, sometimes smelly environment • Must be able to perform tasks such as lifting, walking, climbing, stooping, standing, pushing and/or pulling We will hire and train candidates who are self-motivated. We promote from within and offer excellent growth opportunities for anyone looking for a career not just a job. Benefits Include: • Medical Insurance • Dental Insurance • Vision Insurance • Life Insurance • Long Term Disability • $500 Referral Bonus Program • 401k • 401k Matching • Flexible Spending Account (FSA) • Employee Assistance Program (EAP) • Tuition Reimbursement We comply with E-Verify, Background Checks and Drug Screens. Thank you for your interest in joining the CAPTEK team. You will be contacted shortly if your application is selected.
General Atomics Aeronautical Systems, Inc. (GA-ASI), an affiliate of General Atomics, is a world leader in proven, reliable remotely piloted aircraft and tactical reconnaissance radars, as well as advanced high-resolution surveillance systems. Under minimal supervision, this position is responsible for performing a variety of non-routine and non-repetitive assembly operations on electronic and /or mechanical assemblies and subassemblies. Determines and/or follows methods and sequence of operations in performing assembly tasks such as wiring, component installation, hand soldering and cable harnessing on assembly units. Makes continuity checks on work in process and completed work. May monitor and verify quality in accordance with control procedures. DUTIES & RESPONSIBILITIES: Assembles components, assemblies or sub-assemblies. Makes setups and adjustments holding tolerances to specifications. May perform duties as required in assembly of electronic equipment such as cables, harnesses, chassis, and printed circuit boards; or may perform mechanical assembly of panels, LRU's, batteries, and servo motors as it pertains to cable assembly. May disassemble, modify, rework, reassemble and test experimental/prototype assemblies or subassemblies according to specifications. Responsible for observing all laws, regulations and other applicable obligations wherever and whenever business is conducted on behalf of the Company. Expected to work in a safe manner in accordance with established operating procedures and practices. Completes Disposition on Nonconforming product when needed. Participates in production Integrated Process Team (IPT) Communicates/works with engineering and other support departments. Participates/runs weekly cell team meeting. Mentors team members in assigned cell. Assist team/assemblers in building and solving technical issues of cable assembly. Additional Functions: Performs 5S housekeeping and cleanup duties upon completion of assigned tasks Supports Clean-as-you-go cleanup duties during the shift. May train lower level assemblers or act as a lead and direct the work of others. 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. 50196 Job Qualifications: Typical requires a high school diploma or equivalent and seven or more years experience. Must be customer focused and possess: The ability to read and interpret engineering drawing and wire lists. Extensive knowledge in specialized functions. A comprehensive understanding of the general and specific aspects and technical phase of the job and their practical to complex applications to intricate problems. Good knowledge of computer operations and applications pertinent to the position. Familiarity with use of soldering and compression connection tools. Good visual perception and ability to distinguish between colors. The ability to work independently or in a team environment is essential as is the ability to work extended hours as required. Ability to obtain and maintain DoD Security clearance is required. Salary:$52,020 - $77,325Travel Percentage Required 0 - 25Relocation Assistance Provided Not Provided US Citizenship Required? YesClearance Required? Desired Clearance LevelMid-Level (3-7 years) WorkstyleOnsite