Associate QC Biochemist

The Associate QC Biochemist performs compendial method testing sample management and stability management for biopharmaceutical products. Additional responsibilities include equipment management and laboratory duties

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This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:

• Performs routine compendial testing (visual inspection pH osmolality residual moisture subvisible particulate matter) per SOP and GMP and utilizes electronic management systems in daily operations.

• Performs sample aliquoting on stability samples coordinates sample shipments (reference standard critical reagents etc) and performs annual inventory inspections (reference standard stability retains) with proper GMP documentation. Option to learn to support small batch aseptic product stability fills as a runner and/ or assists with aseptic product reference standard fills.

• Performs laboratory duties and safety checks following all safety GMP CFR and other regulations in order to assure laboratory compliance.

• Assists in laboratory investigations and assay troubleshooting with supervisor/ manager.

• Evaluates laboratory SOPs and recommends improvement opportunities to maintain compliance with corporate and regulatory guidelines. Revises laboratory SOPs and WIs as assigned.

• Performs data verification for use in stability reports and responsible for updating stability data tables and trends as assigned.

• Operates and maintains QC laboratory equipment/ instrument per GMP including responsibilities for installing / deactivating equipment/ instrument per GMP procedures as assigned.

• Participates in the on-call response team for chamber excursions.

• Trained as a Self-Inspector Auditor and participates in department Self Inspections as assigned.

• Able to work effectively as part of a team and exhibit effective interpersonal skills.

Why you

Basic Qualifications:

We are looking for professionals with these required skills to achieve our goals:

• B.S. / B.A. degree in Chemistry Biochemistry or Biology

• This role is on-site at our United States facility. require occasional work outside standard hours for on-call duties.

Preferred Qualifications:

If you have the following characteristics it would be a plus:

• Ability to work both individually and as part of a team with very good communication skills (verbal and written).
• Strong organizational skills and effectively meets timelines

• Experience in s cGMP regulated environment

• Experience working with standard operating procedures

Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees.

Why GSK

Uniting science technology and talent to get ahead of disease together.

GSK is a global biopharma company with a purpose to unite science technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade as a successful growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory immunology and inflammation; oncology; HIV; and infectious diseases to impact health at scale.

People and patients around the world count on the medicines and vaccines we make so were committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients accountable for impact and doing the right thing is the foundation for how together we deliver for patients shareholders and our people.

Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us at where you can also request a call.

Please note should your inquiry not relate to adjustments we will not be able to support you through these channels. However we have created a Recruitment FAQ guide. Click the link where you will find answers to multiple questions we receive

GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race color religion sex (including pregnancy gender identity and sexual orientation) parental status national origin age disability genetic information (including family medical history) military service or any basis prohibited under federal state or local law.

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GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSKs commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.

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