Pharma Laboratory Scientist - GMP Compliance

Pharma Laboratory Scientist - GMP Compliance

Location : Coral Springs, FL

Type of Work : On Site

Schedule : First shift (09 : 00am-06 : 00PM) l ( Second Shift (2 : 00 PM 11 : 00 PM)

Type of Contract : Temp-to-Perm

Pay Rate : Competitive commensurate with experience and technical proficiency

Description

A fast-growing pharmaceutical manufacturer is seeking motivated Scientists I and II to support its GMP analytical and formulation laboratories.

These are hands-on roles that require direct experience with chromatographic systems (HPLC, UPLC, GC) and analytical documentation in a GMP-regulated environment.

Successful candidates will demonstrate exceptional command of Good Documentation Practices (GDP), attention to detail, and the ability to perform and review data with minimal supervision.

Responsibilities and Duties

Perform routine and non-routine analytical testing of raw materials, in-process samples and finished products in compliance with GMP.

Operate and maintain analytical instrumentation (HPLC, UPLC, GC) and related software (Empower).

Ensure all laboratory records follow Good Documentation Practices (GDP) and data integrity requirements.

Prepare protocols, reports and SOPs in alignment with internal quality systems and regulatory guidelines.

Support investigations of OOS / OOT, deviations, and CAPA activities with accurate analytical input.

Participate in method transfer, verification and validation activities as assigned.

Review peer data for accuracy and completeness; conduct analytical or data review when qualified.

Support introduction of new technologies and continuous improvement initiatives within the laboratory.

Maintain a safe work environment and comply with EH&S and corporate policies.

Requirements

Education :

BS in Chemistry, Biochemistry, Pharmaceutical Sciences or related discipline (Scientist I).

MS or higher preferred for Scientist II and Senior levels.

Experience :

Minimum 1 year of direct GMP laboratory experience (Associate / Scientist I).

Minimum 3 years of hands-on experience in a pharmaceutical GMP analytical laboratory.

Must demonstrate hands-on experience in chromatography (HPLC, UPLC, GC).

Technical Proficiency :

Direct experience with GMP / GLP, USP, and ICH guidelines (MANDATORY).

Exposure to Empower software for data acquisition and reporting.

Solid understanding of Good Documentation Practices (GDP) and data integrity standards.

Exposure to CAPA, deviation, and OOS / OOT investigations.

Preferred :

Experience in data analysis or peer review is a plus.

Experience supporting method validation or transfer projects.

Prior exposure to regulated audits (FDA, EMA, MHRA).

ttg Talent Solutions is an Equal Opportunity Employer and recruiting agency. We are committed to creating an inclusive and diverse work environment and welcome applications from all qualified candidates regardless of race, color, religion, gender, sexual orientation, national origin, age, disability, or veteran status. Please note that all offers of employment are contingent upon the successful completion of a drug test and background check. We maintain a drug- and substance-free workplace to ensure the safety and well-being of all employees.

At ttg, We believe in making a difference One Person at a Time, ttg OPT.

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