Supervisor, Quality Assurance - 1st Shift Monday to Friday

Amneal Pharmaceuticals

Brookhaven (NY)

On-site

USD 90,000 - 105,000

Full time

14 days+

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Benefits offered by this job

Comprehensive health benefits

401(k) matching

Employee well-being programs

Job summary

Amneal Pharmaceuticals is seeking a Supervisor for Quality Assurance to oversee daily priorities in quality operations and ensure compliance with standards in pharmaceutical manufacturing. The ideal candidate will possess a relevant degree and supervisory experience, along with strong leadership and communication skills. This position offers a competitive salary and benefits, emphasizing employee well-being and growth opportunities within the company.

Qualifications

Supervisor with experience in Quality Assurance.
Education in technical fields is preferred.
Experience in pharmaceutical or manufacturing environments.

Responsibilities

Schedules and coordinates daily priorities for QA operations.
Trains and supervises QA team to ensure compliance.
Monitors stages of QA to ensure GMP/SOP compliance.

Skills

Leadership

Adaptability

Communication

Problem Solving

Multitasking

Education

Bachelor's Degree in Chemistry, Biology, or related technical field

Associate Degree in Pharmaceutical or related field with 2 years experience

High School or GED with 5 years experience

Tools

Microsoft Office

Job description

Supervisor, Quality Assurance - 1st Shift Monday to Friday

1 week ago Be among the first 25 applicants

Description:

The Supervisor, Quality Assurance, schedules and coordinates daily priorities for incoming raw materials and labeling components, in-process testing, finished product sampling, in-process labeling and packaging operations, sampling and inspection activities on all work shifts.

Schedule:

1st Shift - 7am - 3:30pm Monday to Friday w/ shared Saturdays on Rotation Schedule

Essential Functions:

Responsible for scheduling and coordinating daily priorities for incoming raw material, in-process material, finished product and in-process packaging/labeling operations sampling and inspection activities.
Trains, supervises and evaluates the performance of QA inspectors, QA Specialist and QA Auditors to assure compliance with Standard Operating Procedures (SOPs)/cGMP.
Responsible for final product: Monitors all stages of QA in-process/packaging operations to ensure strict compliance with cGMP/SOPs.
Assists management with the development of new and revised SOPs, executes validation & qualification studies, performs investigations and other assignments as required.
Handles Change Controls, Deviations, Corrective Actions and Preventative Actions (CAPA) through effective quality management tools.
Handles customer complaints to include retrieval of samples, performing applicable tests, preparation of reports and submission before due date.
Monitors and ensures that batch records are audited per manufacturing/packaging/shipping requirements, when required.
Conducts internal audits for compliance with SOP, cGMP & FDA requirements.

Additional Responsibilities:

Initiates, investigates and completes CAPA for all QA unplanned deviations under the guidance of QA Manager.
Writes, reviews and revises SOPs as directed by QA Manager/Director.
Plans, monitors and supervises cross training of all QA Inspectors.
Monitors absences and prepares Kronos, HR requestions/data change forms for all shift personnel, whenever required.
Reviews performance of all QA Inspectors in the shift as and when directed by HR.

Education:

Bachelors Degree (BA/BS) Preferred degree in Chemistry, Biology or other related technical field - Preferred
Associate Degree Pharmaceutical or related degree with 2 years Pharmaceutical/Manufacturing experience including 2 years supervising staff or working in a lead role. - Preferred
High School or GED General/HS Curriculum with 5 years pharmaceutical/Manufacturing Experience, including 3+ supervising staff or working in a lead role. - Required

Experience:

1 year or more in With a BA/BS -Pharmaceutical/Manufacturing experience including 1+ supervising staff or working in a lead role.
2 years or more in With an AA/AS Pharmaceutical or related degree with 5 years Pharmaceutical/Manufacturing experience including 2+ supervising staff or working in a lead role.
3 years or more in HS/GED with 3 years pharmaceutical/Manufacturing Experience, including 5+ supervising staff or working in a lead role.

Skills:

To be a team leader and player who can successfully meet the organization's goals within a stipulated time frame. - Intermediate
Must be able to multitask and adapt to a rapidly changing environment. - Intermediate
Strong communication and writing skills. - Intermediate
Must be able to problem solve and make decisions with limited supervision. - Intermediate
Must be able to lead, coach and supervise the team with flexibility. - Intermediate
Microsoft Office; able to learn in-house computer systems and software. - Intermediate

Specialized Knowledge:

Knowledge of cGMPs.

The base salary for this position ranges from $90,000 to $105,000 per hour. Amneal ranges reflect the Company’s good faith estimate of base salary that Amneal reasonably believes that it will pay for said position at the time of the posting. Individual compensation will ultimately be determined based on a variety of relevant factors, including but not limited to, qualifications, geographic location and other relevant skills. At the heart of our Total Rewards commitment is a comprehensive, flexible and competitive benefits program for eligible positions that enables you to choose the plans and coverage that meet your personal needs. This includes above-market, diverse and robust health and insurance benefits to meet the varied needs of our employees as well as a significant 401(k) matching contribution to help our employees save for retirement. We also promote employee well-being with programs that helps you enjoy your career alongside life’s many other commitments and opportunities.

Amneal is an Equal Opportunity Employer that does not discriminate on the basis of sex, age, race, color, creed, religion, national origin, sexual orientation, gender identity, genetic information, disability, veteran status, liability for service in the U.S. Armed Forces or any other characteristic protected by applicable federal, state, or local laws.

Seniority level