Manufacturing Superintendent
A Little About Us:
At BIOVECTRA, we are passionate about improving patient care by manufacturing better therapeutics. As a contract drug manufacturing organization (CDMO), we partner with leading pharmaceutical and biotech companies worldwide. Our team combines a global reach with a strong sense of community, fostering a workplace built on teamwork, respect, professionalism, and quality. We embrace diversity and strive to maintain a welcoming and inclusive environment.
About the Role:
We are seeking a dynamic and experienced Manufacturing Superintendent to join our team. Someone who can demonstrate emotional and organizational intelligence, diversity, the ability to develop others, and who can facilitate transformation. This role is responsible for supervising and leading a pharmaceutical manufacturing team in GMP production, purification, isolation, and packaging of synthetic chemical, natural extraction, and fermentation-related products. The successful candidate will ensure adherence to safety practices, company protocols, and operational objectives in a fast-paced, multi-product manufacturing environment.
Key Responsibilities:
- Oversee Team Leads to ensure production goals and quality standards are met.
- Mentor and develop team members, providing constructive feedback and training. Manage employee schedules, payroll, and compliance with workplace policies.
- Review completed Batch Production Records (BPRs) for accuracy and compliance.
- Assist in updating and optimizing BPRs and work instructions to improve efficiency.
- Maintain manufacturing schedules through proper documentation and material staging.
- Ensure all manufacturing documents are current and compliant.
- Monitor and maintain processing equipment and production areas to meet schedule demands.
- Identify and resolve equipment, process, and facility issues; participate in process risk assessments.
- Support the hiring, training, and performance evaluation of employees.
- Prepare for and participate in regulatory inspections and audits.
- Ensure workplace compliance with safety and operational standards.
- Collaborate with multi-disciplinary teams to uphold product quality and timely delivery.
- Provide after-hours consultation during manufacturing activities when required.
- Participate in client meetings and teleconferences.
- Perform hands-on manufacturing operations as needed.
Enough about us. Let's Talk About You!
What You Bring to the Role:
· Post-secondary degree or diploma in a scientific field is an asset.
· 2 years of demonstrated leadership experience
· 5 years of technical experience.
· Familiarity with GMP protocols and FDA guidelines.
· Strong communication, problem-solving, and leadership skills.
· Ability to work in a dynamic, project-driven team environment.
· Broad-based technical knowledge of process equipment.
· High level of independence, maturity, and decision-making ability.
· Ability to shift priorities and reallocate resources efficiently.
Why Join BIOVECTRA?
BIOVECTRA offers a competitive salary and benefits package including a healthcare and personal health spending account. You will have opportunities for professional growth in a collaborative and dynamic work environment.
If you are a motivated manufacturing professional looking for a challenging and rewarding career, we encourage you to apply.
How to Apply:
Interested candidates are invited to apply by clicking the "Apply Now" button below. We thank all applicants for their interest; however, only those selected for an interview will be contacted.