QA Specialist at Eurofins in Sanford, North Carolina

Job Description:

Company Description



The work we do at Eurofins matters, and so do our employees. At Eurofins, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.


Eurofins 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 works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.


If you're looking for a rewarding career, a place to call home, apply with us today!



Job Description




POSITION SUMMARY:



This position provides Quality Assurance oversight for Quality Control (QC). Provide QA (Quality Assurance) review and approval of Quality method validation/ QC equipment qualification, QC protocol, reports, QC process control document, new and existing procedures, and Quality Control deviation/investigations. Supports process improvements implementation.



POSITION RESPONSIBILITIES:

• Perform QA technical review for assigned areas such as Validation documents, Method transfer Protocol amongst others.


• Provide final QA approval on simple change control, effectiveness check, CAPA implementations, compendial assessments, and other documents associated with the business unit.


• May also review and approve documents such as Deviation, complaints investigations, Laboratory investigations (OOS/OOT/OOE), and other Quality Events/Lab Events, Electronic build of Master Batch or any electronic record when needed, and all associated to compendial changes.


• Capable to Make quality decisions in real time according to regulations and procedures.


• Ability to work collaboratively with internal partners to resolve technical issues.


• Willing to perform other duties as assigned and take ownership to support the implementation of activities needed for the start-up.

Qualifications




BASIC MINIMUM QUALIFICATIONS:

• Bachelor's Degree in relatable field (Microbiology, Chemistry, Pharmaceuticals, etc.)


• Ability to be problem-solving and analytical skills.


• Familiarized with Pharmacopeia and Regulatory Requirements.


• Attention to detail and the ability to work independently.


• Experience in Quality Control Laboratory cGMP's Laboratory environment.


• Proven ability to work in a team environment through conflict resolution and negotiation.


• Provides excellent communication, writing, and analytical skills.

PREFERRED QUALIFICATIONS:

• 2 - 5 years of manufacturing, laboratory, quality, technical or engineering experience within biotech of the pharmaceutical industry with a BS/BA Degree in Science / related / Field.


• Familiarized and experienced in Pharmacopeia requirements. (e.g., USP, JP, EMEA amongst others)


• Familiarization with the Data Integrity requirements.


• 2 - 5 years of experience such as deviations, Change Controls, Stability Protocols, and all the implementation activities. Support in CAPA closures, Effectiveness checks, and experience in Root Cause Analysis tools.


• At least 2 - 5 yrs. of experience in a quality assurance role, preferably in Quality Assurance for a Quality Control role in the document such as: (e.g., OOS (Out of Specification), OOE (Out of Expectation), OOT (Out of Trend) investigation, specification, method transfer protocol, stability protocol, and others).

Additional Information



Position isFull Time, Monday-Friday, 8:00am-5:00pm
.Candidates currently living within a commutable distance ofSanford
, NCare encouraged to apply. Excellent full-time benefits including comprehensive medical coverage, dental, and vision options.

• Excellent full-time benefits including comprehensive medical coverage, dental, and vision options


• Life and disability insurance


• 401(k) with company match


• Paid vacation and holidays


• Eligibility for potential yearly Bonus & Merit-Based Pay Increases

Eurofins is aM/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

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