Sr. Analytical Scientist - Method Transfer

ZipRecruiter; Philadelphia (Philadelphia County); On-site; USD 70,000 - 95,000; Full time

Job summary

A leading life sciences company offers a position for a Senior Quality Control Analyst in Philadelphia. The role involves method validation and compliance within the QC department, requiring a strong background in biological or chemical sciences and hands-on laboratory experience. Excellent benefits and career growth opportunities are available.

Benefits

Comprehensive medical coverage

Dental and vision options

401(k) with company match

Paid vacation and holidays

Yearly goal-based bonus

Qualifications

• Minimum 5+ years related laboratory experience in the pharmaceutical industry.
• Experience in a GMP environment required.
• Hands-on experience in various assays.

Responsibilities

• Lead method validation activities and ensure compliance with QC processes.
• Author GMP documents and conduct complex deviation reports.
• Interface with other departments and provide QC ownership.

Skills

HPLC

qPCR

PCR

mammalian cell culture techniques

tissue-culture assays

ELISAs

Western blots

Education

BS degree in biological or chemical sciences

Tools

agarose gel electrophoresis

protein gel electrophoresis

silver staining

Job description

Job DescriptionJob DescriptionCompany Description

The work we do at Eurofins Professional Scientific Services matters, and so do our employees. At Eurofins PSS, 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 Overview:

The Senior Quality Control Analyst will be responsible for conducting development, validation, routine testing and GMP review of analytical assays in compliance with all applicable quality systems and current cGMPs within the Quality Control department. They will operate as a core member of project teams to support improvements to QC systems and processes including assay performance, improving compliance, and efficiency. The primary goals of this team areto lead the execution of release and stability testing for commercial and clinical GMP, execute assay validation and assay transfer studies and critical reagent qualification studies; the implementation and maintenance of laboratory control procedures and compliance; raw materials and laboratory investigations.

Job Duties:

• Lead method validation activities prior to the Gene Therapy Innovation Center's(GTIC) transfer to support the GTIC Validation Master Plan.
• Lead change controls for method revisions post validation to ensure continued performance of test methods in support of asset post-PPQ prior to GTIC method transfer
• Author (review/approve) and execute method transfer protocols to ensure analytical QC readiness at GTIC in line with GTIC manufacturing and project timelines
• Support of CQV activities in GTIC by providing QC ownership on documents such as IQ/OQ
• Lead bridging activities for equipment changes in support of GTIC readiness prior to equipment purchase to support facility and laboratory start-up
• Lead training strategy and serve as the SME for training of new employees and contractors in associated methods for GTIC readiness.
• Performs quantitative analytical assays asroutine testing in support of release and stability studies
• Acts as a resource to junior QC analysts (and contractors), both from a technical and GMP-compliance standpoint.
• Participate in establishing and maintaining laboratory systems and controls. Active in maintaining the compliance of the laboratory
• Author GMP documents such as analytical methods/forms, technical protocols/reports, CAPAs, and change controls
• Independently complete complex deviation reports and investigations
• Conduct wide variety of assays or tests required to characterize and qualify assay-specific reagents, such as qPCR primers and probes.
• Provide routine support and communication to groups external to QC. Interfaces with other departments within the organization and participates on project teams. Act as a delegate for the QC Lead/Leader at meetings, including GTIC project.
• With guidance, act as the Subject Matter Expert during regulatory audits for their respective assays and will interact directly with regulatory auditors.

Qualifications

Basic Minimum Qualifications:

• BS degree in the biological or chemical sciences with a minimum of 5+ years related laboratory experience in the pharmaceutical industry
• Experience working in a GMP environment is required
• Hands on experience in assays including: HPLC, qPCR, PCR, mammalian cell culture techniques, tissue-culture assays, ELISAs, Western blots,agarose gel electrophoresis, protein gel electrophoresis, silver staining,etc.

Additional Information

Position isFull Time, Monday-Friday, 8am-5pm with overtime as needed.Candidates currently living within a commutable distance toPhiladelphia, PAare encouraged to apply.

What we offer:

• Excellent full time benefits including comprehensive medical coverage, dental, and vision options
• Life and insurance
• 401(k) with company match
• Paid vacation and holidays
• Yearly goal-based bonus & eligibility for merit-based increases

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.