Use Your Power for Purpose

Every day our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible innovative and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development maintenance compliance or research analysis your contributions have a direct impact on patient care. By being part of our team you help uphold a quality culture that adapts and evolves to meet the needs of patients ensuring that every product we deliver is of the highest standard.

What You Will Achieve

In this role you will:

• Perform various chemical tests such as water analysis FTIR ID HPLC and other compendial assays.

• Write and perform raw material verification protocols and associated reports.

• Ensure training records are updated and correctly filed to reflect current testing capabilities.

• Interpret and evaluate data for accuracy precision trends and potential cGMP impact recommending appropriate corrective actions.

• Ensure all documentation and quality records comply with Good Manufacturing Practices and Good Laboratory Practices and are filed according to existing policies.

• Review and revise Standard Operating Procedures analytical methods and related documents to keep them current.

• Conduct analyses on finished products raw materials and components including data entry review and approval in a computerized database.

• Contribute to the completion of complex projects manage time effectively to meet targets and develop plans for work activities within a team while exercising judgment with reliance on manager and working under their direction.

• Working knowledge of compendial testing/requirements is preferred.

Here Is What You Need (Minimum Requirements)

• Applicant must have a bachelors degree with 0 years of experience; OR an associates degree with 4 years of experience; OR a high school diploma (or equivalent) and 6 years of relevant experience

• Experience with analytical laboratory techniques/technologies

• Experience with raw material enrollments

• Knowledge of GMP guidelines

• Knowledge and experience with Quality Systems

• Strategic and Innovative Thinking

• Expertise with analytical techniques such as: compendial testing FTIR GC HPLC etc.

• Problem Solving and Critical Thinking Skills

• Good Communication Skills

Bonus Points If You Have (Preferred Requirements)

• Experience with using HPLC (High Pressure Liquid Chromatography) techniques

• Proven track record in leading continuous improvement projects

• Strong knowledge of lean manufacturing principles six sigma methodologies and statistical analysis

• Strong problem-solving skills and attention to detail

• Ability to manage multiple priorities and meet deadlines.

• Excellent interpersonal skills and the ability to communicate effectively with colleagues at all levels

• Adaptability and willingness to learn new techniques and procedures

• Experience using common AI tools including generative technologies such as ChatGPT or Microsoft Copilot to support problem solving and enhance productivity. Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices including risk management and ethical use

PHYSICAL/MENTAL REQUIREMENTS

• Ability to lift carry push or pull materials weighing up to20 pounds.

• Ability to work in alaboratory environment

NON-STANDARD WORK SCHEDULE TRAVEL OR ENVIRONMENT REQUIREMENTS

• This role is standard day Monday through Friday work shift

Other Job Details:

• Last day to Apply:May 5th 2026.

• Work Location Assignment:On Premise

Relocation assistance may be available based on business needs and/or eligibility.

Candidates must be authorized to be employed in the U.S. by any employer.

U.S. work visa sponsorship (such as TN O-1 H-1B etc.) is not available for this role now or in the future.