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QC Associate 1 - Raw Materials/Water
Sanford, NC 27330
12 Months, Contract
On-site
Job Summary
- Job Title:
- QC Associate 1 - Raw Materials/Water
- Posted Date:
- Aug 22, 2025
- Duration:
- 12 Months, Contract
- Shift(s):
-
08:00 - 16:00
- We care about you! Explore Rangam’s benefits information
Talk to our Recruiter
- Name:
- Satnam Singh
- Email:
- satnam@rangam.com
- Phone:
- 513-447-8917
Description
Rangam is seeking candidates for a Contract role as a QC Associate 1 - Raw Materials/Water with our client Pfizer, one of the world’s largest pharmaceutical companies. Seeking candidates in Sanford NC or willing to relocate.
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.
- Perform sampling and labeling of materials as per defined procedures and verify all equipment and instruments.
- 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 supervisor and working under their direction.
Here Is What You Need (Minimum 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
- Demonstrated technical skills in chemistry laboratory testing
- Ability to read and understand applicable compendial methods, Standard Operating Procedures, technical procedures, and governmental regulations
- Knowledge of Good Manufacturing Practices and its application standards, processes, and policies.
- Excellent organizational skills and strong ability to multi-task
- Strong written and verbal communication skills
- Proficiency with unique Quality Control instruments to meet accuracy specifications for sample management, retains management, interpretation, and evaluation
Bonus Points If You Have (Preferred Requirements)
- Experience with laboratory work, particularly using analytical techniques such as HPLC, pH, Polarimetry, etc.
- 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 procedure.
Physical/Mental Requirements
- Non-existent to minimal travel.
- Must be able to wear appropriate PPE (e.g., lab coat, safety glasses, non-porous shoes, gloves, etc.)
- Ability to lift 30 lbs, stand for 2 to 3 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.
Work Location Assignment: On Premise
- Perform tasks associated with maintaining Good Manufacturing Practices (cGMP) compliant Quality Control and Stability laboratories.
- Support environmental monitoring/water testing in the QC Raw materials laboratory.
- Test incoming raw materials per compendial methods.
- Follow Environment Health and Safety requirements for site and QC laboratories.
- Support product transfers, new product development, regulatory queries, cost improvement projects, and Drug Product plant support for Cleaning Validation.
- Operate within established HR policies and basic colleague relations guidelines.
- Write Standard Operating Procedures (SOPs), technical reports, project plans, etc.
Hard Skills:
- Lab Exp
- Degree in Life/Phys sciences
- Analytical
- Ishihara Test (color)
Sunshine Act
Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.
EEO & Employment Eligibility
It is the policy of Rangam Consultants, Inc. to provide equal employment opportunities to all applicants and employees without regard to any legally protected status such as race, color, religion, gender, national origin, age, disability or veteran status.
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