Production Supervisor- 2nd Shift

ALMAC Group; Lower Providence Township (PA); On-site; USD 65,000 - 85,000; Full time

Benefits offered by this job

Medical benefits

Vision benefits

Dental benefits

PTO 20 days per year

12 holidays per year

Disability & Life Insurance

401k company match

Professional development

Job summary

Almac Group is seeking a 2nd Shift Production Supervisor to lead day-to-day production activities in our Pennsylvania facility. You will ensure on-time, compliant packaging of pharmaceutical dosage forms and efficient staffing to meet the master production schedule.

Required 3–5 years in production and a high school diploma; bachelor's degree preferred. Experience in GMP environments and strong leadership are highly valued.

Qualifications

• 3 to 5 years' experience in production environment.
• High School Diploma or GED.
• Bachelor's Degree preferred.
• Pharmaceutical GMP environment experience preferred.
• Supervisory experience preferred (not necessarily in pharma).
• Strong leadership and change-management capabilities.
• Excellent interpersonal skills and ability to drive change.

Responsibilities

• Supervise, organize, monitor, and ensure SOP and cGMP compliance of production personnel.
• Oversee packaging of pharmaceutical dosage forms using equipment (bottle filling, blister cards, labeling, kit assembly, pouching).
• Allocate personnel to scheduled operations and support adherence to the master production schedule.

Skills

Production supervision

Leadership

Change management

GMP experience

SOP compliance

Education

High School Diploma or GED

Bachelor's Degree

Tools

ERP/Inventory systems

Job description

Almac Group is growing-and we're looking for leaders ready to grow with us!

The 2nd Shift Production Supervisor is responsible for management of all day-to-day activities within the Production shift, ensuring all assigned tasks are delivered on time, according to specification and within budget. Responsibilities include but are not limited to:

• Responsible for providing supervision, organization, monitoring and SOP and cGMP compliance of production personnel.


• The Production Supervisor is responsible for the successful, cost effective and timely packaging of pharmaceutical dosage forms utilizing various packaging equipment including but not limited to bottle filling, blister card packaging, vial & ampoule labelling, kit assembly and pouching operations.


• The Production Supervisor is responsible for allocation of production personnel to scheduled operations ensuring adherence to the master production schedule and providing direction to staff in resolving production-related problems.

Essential Functions

• The Production Supervisor is responsible for providing supervision, organization, monitoring and SOP and cGMP compliance of production personnel.


• The Production Supervisor is responsible for the successful, cost effective and timely packaging of pharmaceutical dosage forms utilizing various packaging equipment including but not limited to bottle filling, blister card packaging, vial & ampoule labelling, kit assembly and pouching operations.


• The Production Supervisor is responsible for allocation of production personnel to scheduled operations ensuring adherence to the master production schedule and providing direction to staff in resolving production-related problems.


• The Production Supervisor is responsible for oversight of executed batch documents including issuance, reconciliation, recording of finished product, and required inspections using the inventory system and manually recording required details in the batch document according to appropriate Almac Standard Operating Procedures (SOP's) and current Good Manufacturing Practices (cGMP's).

Second shift is 2nd Shift Role 230-1030pm

Qualifications

Required Experience:

• 3 to 5 years' experience in production environment

Required Education:

• High School Diploma or GED

Preferred Education:

• Bachelor's Degree

Preferred Experience:

• Pharmaceutical or similar GMP environment


• Supervisory experience (not required to be in Pharmaceutical)


• A demonstrable track record of success delivering continuous improvement/OEE practices whilst adhering to strong management and leadership principles.


• Excellent interpersonal skills and experience of successfully delivering change management programs to improve efficiencies are essential.


• Proven ability to work well under pressure and able to priorities workloads.

Required Knowledge:

• Familiarity with team-based manufacturing environment

Preferred Knowledge:

• Pharmaceutical or similar GMP environment


• ERP/Inventory systems


• Label generation

What can Almac Group offer you?

• Medical, Vision & Dental benefits from the 1st of the month following start date


• 20 days PTO per year, accrued monthly following start date


• 12 holidays per year


• Company paid Long and Short-term disability along with Life Insurance


• 401k company contribution


• Professional development programs/ continuous learning opportunities

Almac is an exceptional, award winning, drug development solutions provider at the forefront of the pharmaceutical industry. We are a privately owned organization that has organically grown over 50 years now employing 7,500 highly skilled personnel worldwide. Our US Headquarters is located at Souderton, PA with additional operations scattered around the US and Europe. 'Partnering to Advance Human Health' is more than just a tagline - it is our way of life.

Embracing diversity is at the heart of enhancing Almac Group's unique culture and reflects our fundamental belief that all people deserve equality, inclusivity and the opportunity for advancement. We are committed to cultivating a welcoming, supportive, and inclusive environment for all. Together, we will build on the strength in our diversity and deliver exceptional solutions to advance human health globally.

Almac Group, Inc. is an Equal Opportunity Employer - Minorities/Women/Protected Veterans/Disabled - Proudly embracing diversity in all of its expressions.

Almac provides reasonable accommodations to people with disabilities who need assistance completing the application process. Please email us at [e-mail] to request assistance.