Bioprocess Technician III and IV (Nights, 6pm to 6am
Listed on 2026-08-09
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Quality Assurance - QA/QC
Quality Engineering
Rangam is seeking candidates for a Direct Hire role as a Bioprocess Technician IV- 6pm to 6am with our client, one of the world’s largest pharmaceutical companies. Seeking candidates in Sanford, NC or willing to relocate.
Our breakthroughs would not reach the hands of patients without our dedicated pharmaceutical manufacturing team. We rely on agile members who understand the critical impact of their role in client's mission. Patients need colleagues like you who take pride in their work and continuously strive to improve outcomes. Your efforts ensure that patients and physicians have timely access to the medicines they need.
WhatYou Will Achieve
- Operate, service, adjust, clean, and sterilize production-related equipment in compliance with cGMPs and safety regulations.
- Maintain a clean room environment and complete work instructions to meet regulatory requirements.
- Ensure equipment functionality, report or correct malfunctions, and assist in complex setup or repair operations.
- Manage time effectively, focus on professional development, and take accountability for results.
- Prioritize workflow, assist less-experienced colleagues, and adhere to quality standards and best practices.
- Maintain accurate documentation, including training records, batch records, check sheets, and log books.
- Support audits, help close audit observations, and utilize automated and enterprise systems to perform tasks.
- Communicate cross-functionally with technology transfer teams, lab scientists, supply chain, quality, and engineering.
- Take responsibility for individual contributions to team deliverables, represent the work group, and foster a positive team environment.
- Complete assignments based on established procedures, identify process improvements, troubleshoot issues, and provide direction and training to team members.
- High School Diploma or GED
- 4+ years of experience, particularly in a pharmaceutical or other cGMP (Current Good Manufacturing Practices) environment
- Effective verbal and written communication
- Proficiency in operating and troubleshooting production equipment
- Strong understanding of cGMP and safety regulations
- Ability to maintain accurate documentation and records
- Experience in a clean room environment
- Competence in using automated and enterprise systems
- Effective cross-functional communication skills.
- Basic mechanical knowledge and hands-on experience using various hand tools
- Experience in a pharmaceutical manufacturing environment
- Knowledge of process improvement methodologies
- Ability to train and mentor less-experienced colleagues
- Ability to work independently and as part of a team
- Attention to detail and commitment to quality
- Adaptability and flexibility in a dynamic work environment
- Familiarity and basic understanding of common AI tools and a curiosity for learning how they can be used to enhance productivity.
- Last day to apply:
August 4
The salary for this position ranges from $25.88 to $43.14 per hour. In addition, this position offers eligibility for overtime, weekend, holiday and other pay premiums depending on the work schedule and the Company’s policies.
We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments.
Benefits offered include:
- 401(k) plan with client's Matching Contributions and an additional client's Retirement Savings Contribution
- paid vacation, holiday and personal days
- paid caregiver/parental and medical leave
- health benefits to include medical, prescription drug, dental and vision coverage
Learn more at client's Candidate Site – U.S. Benefits | (uscandidates.my**).
Compensation structures and benefit packages are aligned based on the location of hire.
The United States salary range provided applies only to the United States
- North Carolina
- Sanford location.
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.
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