Pharmaceutical QA Senior Specialist
2 days ago
Pharmaceutical QA Senior Specialist - Group Leader Eurofins Scientific is an international life sciences company, providing a range of analytical testing services to clients across multiple industries. Our mission is to make life and the environment safer, healthier, and more sustainable. We work with major companies worldwide to ensure product safety, authenticity, and accurate labelling. Our network of over 900 laboratories in more than 54 countries employs 58,000 staff and offers over 200,000 analytical methods to evaluate biological substances and products. Job Description This position oversees Quality Assurance for Quality Control (QC). Responsibilities include reviewing and approving validation/qualification documents, QC protocols, reports, process control documents, procedures, and investigations related to QC. The role supports process improvements and is based in Sanford, NC. Position Responsibilities Perform QA technical reviews for validation documents, transfer protocols, and related areas. Approve change controls, effectiveness checks, CAPAs, and assessments. Review and approve deviation reports, investigations, lab events, electronic records, and related documentation. Make real-time quality decisions in accordance with regulations and procedures. Collaborate with internal teams to resolve technical issues. Support activities for start-up operations and other duties as assigned. Qualifications Bachelor's or Master's Degree in Microbiology, Chemistry, Pharmaceuticals, or related field. Experience: 6-8 years for Bachelor's degree holders; 4-6 years for Master's degree holders. Relevant experience in biotech or pharmaceutical manufacturing, laboratory, quality, or engineering roles. Experience in a cGMP QC laboratory environment. Knowledge of pharmacopeia standards (USP, JP, EMEA), data integrity, deviations, change controls, and CAPA processes. Ability to work collaboratively and make informed quality decisions. Valid drivers license and personal transportation. Additional Information Full-time, Monday-Friday, first shift (8AM-5PM). Candidates in or near Sanford, NC are encouraged to apply. Benefits include medical, dental, vision, life and disability insurance, 401(k) with match, paid vacation and holidays. Eurofins is an Equal Opportunity Employer, supporting diversity and inclusion. #J-18808-Ljbffr
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Pharmaceutical QA/QC Senior Specialist
2 days ago
Sanford, United States Eurofins PSS Insourcing Solutions Full timeEurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier, and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest...
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Pharmaceutical QA/QC Senior Specialist
7 days ago
Sanford, North Carolina, United States Eurofins PSS Insourcing Solutions Full timeJob DescriptionThis role will provide Quality Assurance oversight for Quality Control activities, including review and approval of method validations, equipment qualifications, protocols, reports, procedures, and deviations. The role supports implementation of process improvements.This is on-site in Sanford, NCConduct QA reviews and approvals for validation...
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QA Validation Specialist
3 weeks ago
Sanford, United States SPECTRAFORCE Full timePosition Title: QA Validation SpecialistWork Location: Sanford, NC 27330Assignment Duration: 11 monthsWork Schedule: 8 AM - 4:30 PMWork Arrangement: 100% onsitePosition Summary: The Specialist, QA Validation will be primarily responsible for the implementation, execution and assessment of quality systems, procedures, and records to support compliant GMP...
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Specialist, QA Validation
4 weeks ago
Sanford, United States Planet Pharma Full timePay $76-$81 per hourOn-site Role 1 year extendable contractMedical, Dental, Vision, 401kThe Specialist, QA Validation will be primarily responsible for the implementation, execution and assessment of quality systems, procedures, and records to support compliant GMP operations. This position works closely with Validation, Engineering, Manufacturing, Quality...
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Specialist, QA Validation
4 weeks ago
Sanford, United States Planet Pharma Full timePay $76-$81 per hourOn-site Role 1 year extendable contractMedical, Dental, Vision, 401kThe Specialist, QA Validation will be primarily responsible for the implementation, execution and assessment of quality systems, procedures, and records to support compliant GMP operations. This position works closely with Validation, Engineering, Manufacturing, Quality...
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Specialist, QA Validation
3 weeks ago
Sanford, NC, United States Planet Pharma Full timePay $76-$81 per hour On-site Role 1 year extendable contract Medical, Dental, Vision, 401k The Specialist, QA Validation will be primarily responsible for the implementation, execution and assessment of quality systems, procedures, and records to support compliant GMP operations. This position works closely with Validation, Engineering, Manufacturing,...
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QA Change Control
2 days ago
Sanford, United States Staffing the Universe Full timeQa Change Control This position supports the Pharmaceutical Sanford, NC Quality Assurance department by performing Quality Assurance activities related to change control and validation associated with clinical and commercial products. Colleagues in this role should be able to demonstrate the following:
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QA Validation Specialist
3 weeks ago
Sanford, NC, United States SPECTRAFORCE Full timePosition Title: QA Validation Specialist Work Location: Sanford, NC 27330 most team works 1 day remote) Position Summary: The Specialist, QA Validation will be primarily responsible for the implementation, execution and assessment of quality systems, procedures, and records to support compliant GMP operations. This position works closely with...
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Specialist, QA Validation
3 weeks ago
Sanford, NC, United States Planet Pharma Full timePay $76-$81 per hour On-site Role 1 year extendable contract Medical, Dental, Vision, 401k The Specialist, QA Validation will be primarily responsible for the implementation, execution and assessment of quality systems, procedures, and records to support compliant GMP operations. This position works closely with Validation, Engineering, Manufacturing,...
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QA Associate: Validation
2 days ago
Sanford, United States Belcan Corporation Full timeA leading quality assurance consulting firm is seeking a Quality Assurance Associate in Sanford, NC. The candidate will oversee QA processes to ensure compliance with local and global standards within the biologics manufacturing sector. Responsibilities include reviewing validation documents and authoring quality documents. Ideal candidates should have a...
