Production Technician I - ILP 2nd Shift
About The Position
The Production Technician I supports product visual inspection, labeling, and packaging (ILP) operations at Quva’s facility in Bloomsbury, New Jersey, following established processes and procedures. After completing training, the technician helps ensure medications meet safety, efficacy, and quality standards. The role is safety-sensitive and may be subject to random drug testing in accordance with applicable laws. This is a full-time, onsite, second-shift position with a consistent schedule of Wednesday through Saturday, 3:00 p.m. to 1:30 a.m. Minimum overtime requirements apply. The technician may also support other production areas and shifts as needed.
Requirements
- High school diploma or GED from a recognized institution or organization.
- Pass a color perception exam.
- Pass a vision exam demonstrating 20/20 vision, with or without correction.
- Successfully complete a drug and background check.
- Be at least 18 years of age.
- Be currently authorized to work in the United States on a full-time basis; Quva will not sponsor work visas.
- Strong verbal and written communication skills and ability to work effectively with other departments and people at all levels.
- Working knowledge of cGMPs, regulatory requirements, and applicable SOPs.
- Strong attention to detail; ability to follow policies and procedures and complete administrative tasks correctly and on time.
- Ability to adapt and support multiple production areas and shifts as needed.
Nice To Haves
- Pharmaceutical experience.
- Mechanical aptitude.
Responsibilities
- Assist with preparing inspection and packaging room materials and supplies.
- Conduct labeling and process production materials as required, including primary, secondary, and tertiary product labeling.
- Complete secondary and final product packaging and visually inspect products.
- Clean rooms and equipment daily, bi-weekly, and monthly; complete applicable preventative maintenance forms and checklists in accordance with SOPs.
- Conduct and complete line and room clearances according to established procedures.
- Complete documentation for product accountability and traceability in accordance with Good Documentation Practices, cGMPs, and company ISO standards.
- Comply with 503B guidelines, cGMPs, SOPs, and company policies.
- Perform equipment calibration checks and troubleshoot production equipment as needed.
- Document activities in accordance with established procedures.
- Immediately notify production management of deviations from established processes or procedures.
- Assist other areas as needed, including cleaning, non-sterile filling, kitting, and preparation operations.
- Maintain an inspection-ready environment and support internal and external audits.
Benefits
- Comprehensive health and wellness benefits, including medical, dental, and vision.
- 401(k) retirement program with company match.
- 17 paid days off and 8 paid holidays per year.
- Occasional weekend and overtime opportunities with advance notice.
- Career advancement opportunities at a national, industry-leading, high-growth company.
- Set, full-time, consistent work schedule.
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
High school or GED
