Sr. Associate Scientist - Bioanalytical

Rangam International•Sanford, NC

104d•Onsite

About The Position

Rangam is seeking candidates for a Direct Hire role as a Sr. Associate Scientist - Bioanalytical with our client Pfizer , one of the world's largest pharmaceutical companies. Seeking candidates in Sanford, NC or willing to relocate. Use Your Power for Purpose Every day, Pfizer's unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is both flexible and innovative, always putting the patient first. Whether you are involved in development, maintenance, compliance, or research analysis, your contribution directly impacts patients. In this role, you will: Perform tasks associated with maintaining Good Manufacturing Practices (cGMP) compliant Quality Control and Stability laboratories. Create, review, and approve test method transfer and validation protocols, reports, and equipment qualification records. Maintain compliance with Current Good Manufacturing Practices in Quality Control and Stability laboratories. Support ELISA, plate-based, along with other relevant analytical testing and conduct QC Analytical related investigations. Perform testing on various samples, manage Laboratory Information Management System builds, and review laboratory data. Serve on cross-functional teams, conduct safety inspections, participate in investigations, recommend corrective actions, and train junior colleagues.

Requirements

Applicant must have a Bachelor's degree with 0+ years of experience; OR an Associate's degree with 4 years of experience; OR a High school diploma (or equivalent) and 6 years of relevant experience
Strong technical skills in method validation and QC testing
Experience in QC analytical testing preferably in ELISA and plate-based testing
Deep understanding of pharmaceutical manufacturing, packaging, and quality assurance operations
Detail-oriented with robust knowledge of quality systems
Familiarity with research unit clinical and analytical laboratory environments
Ability to lift 30 lbs, stand for 3 to 4 hours at a time, sit for 2 to 3 hours at a time, walk long distances and bend to obtain items from lower shelving/cabinets.
Intellectual capability to perform complex mathematical problems and perform complex data analysis.
Effective written and verbal communication, as well as interpersonal skills
Strong problem-solving abilities
Effective time management and organizational skills

Nice To Haves

Relevant pharmaceutical experience
Strong understanding of computer system hardware, infrastructure, and networks
Experience with Laboratory Information Management Systems (LIMS)
Proficiency in data analysis and interpretation
Knowledge of regulatory requirements and guidelines
Ability to mentor and train junior colleagues

Responsibilities

Perform tasks associated with maintaining Good Manufacturing Practices (cGMP) compliant Quality Control and Stability laboratories.
Create, review, and approve test method transfer and validation protocols, reports, and equipment qualification records.
Maintain compliance with Current Good Manufacturing Practices in Quality Control and Stability laboratories.
Support ELISA, plate-based, along with other relevant analytical testing and conduct QC Analytical related investigations.
Perform testing on various samples, manage Laboratory Information Management System builds, and review laboratory data.
Serve on cross-functional teams, conduct safety inspections, participate in investigations, recommend corrective actions, and train junior colleagues.

Benefits

Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage.

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