Manufacturing Supervisor Jobs

Supervisor - Manufacturing

📍LEBANON, NEW HAMPSHIRE 📍 (Fully on-site)

**Relocation support is provided**

A thriving Pharmaceutical Manufacturing company has partnered with Charlton Morris to find their next Manufacturing Supervisor.

The Manufacturing Supervisor main purpose is to ensure supervising personnel and operations involved in applicable department. This position requires strict adherence to cGMPs, established manufacturing practices and procedures, and compliance with Quality regulations and guidelines.

🔧Compensation

• Competitive salary + Annual Bonus
• Other tailored company benefits
• Competitive 401K contribution
• Relocation Package

🔧Functions

• Reviews, trains, and develops Manufacturing Technicians in applicable department.
• Provides input during Health Authority inspections.
• Incorporates value improvement programs and new processes from Product Support, Engineering, EH&S, and OE as directed.
• Ensure that the IDP forms include completed learning and aspiration plans and are in place for all reporting personnel to enable the achievement of goals and capability to assume increased levels of responsibility.
• Assures in-process tests are performed in accordance with standard procedures.
• Support evaluation, specification, installation, and validation of new manufacturing equipment as needed.
• Oversees and supervises all manufacturing activities within the department.
• Prepares documentation associated with the job duties of applicable department.
• Ensure that reporting personnel have individual development plans (IDP), with annual goals and measurements that are consistent with the priorities of the business, and that interim reviews are held so that their work is focused on those priorities, and they understand their level of accountability for results and the measurement process.
• Supports manufacturing activities in other departments as instructed by manager.
• Maintains validated systems and re-validates existing systems in accordance validation procedures.
• Assures operations and practices comply with established procedures and records.
• Serves as project member or project leader on improvement programs as needed.
• Performs all job duties and responsibilities in a compliant and ethical manner and in accordance with all applicable healthcare laws, regulations, and industry codes.
• Acquires technical expertise on the function and control of applicable department equipment and techniques related to job function, and regulatory requirements for the operation of the area.

🔧Qualifications and Experience

• Bachelor’s Degree or equivalent experience.
• Excellent communication skills and ability to work in teams also required.
• Minimum five years' manufacturing or process development experience in the pharmaceutical or biotechnology industry.
• Ability to lead people and projects is required.
• Knowledge of bioprocessing and GMPs is essential.

Interested?

Apply directly or reach out at [email protected] 💌

Keywords: downstream, upstream, APIs, protein purification, biopharma, biologics, GMP, bioprocessing