QA Manufacturing Inspector I - 3rd Shift

Cipla; Fall River (MA); On-site; USD 60,000 - 80,000; Full time

Job summary

An established industry player is seeking a dedicated QA Manufacturing Inspector to ensure product quality during the manufacturing process. This role involves conducting in-process testing, performing inspections, and maintaining compliance with Good Manufacturing Practices (cGMP). You will be part of a dynamic team, working closely with quality assurance supervisors to uphold the highest standards of product integrity. If you are detail-oriented, possess strong communication skills, and thrive in a fast-paced environment, this opportunity is perfect for you to make a significant impact in the pharmaceutical industry.

Qualifications

• Minimum high school diploma; vocational training preferred.
• 3+ years of experience in GMP pharmaceutical quality assurance.

Responsibilities

• Monitor product quality during manufacturing processes.
• Conduct in-process testing and inspections as per SOPs.
• Identify and report non-conformances to management.

Skills

Attention to detail

Interpersonal skills

Communication skills

Self-starter

Ability to multitask

Education

High school diploma

Vocational training in pharmaceutical manufacturing

Tools

Microsoft Office

SAP

Job description

QA Manufacturing Inspector I - 3rd Shift

Posting Date: Feb 14, 2025

Country: United States

State: Massachusetts

Location: Fall River

Job Title: QA Manufacturing Inspector - On-the-floor Inspector

FLSA Classification: Full-Time, Non-Exempt/Hourly Professional

Work Location: Fall River, MA

Work Hours: Third Shift: 11:00 PM - 7:30 AM (May vary based on business needs)

Reports To: Quality Assurance Supervisor

PURPOSE

The purpose of the QA Manufacturing Inspector position is to monitor and ensure product quality is maintained throughout all phases of the manufacturing process in compliance with established specifications and standard operating procedures (SOPs).

SCOPE

The scope of this job description is designed to describe the general nature and level of work as well as provide a basic understanding of the role, responsibilities, and expectations of the person assigned to perform the job. This job description is not designed to provide an exact or exhaustive list of all job duties, tasks, skills, and qualifications.

JOB DESCRIPTION

The Quality Assurance (QA) Inspector position is an individual contributor role and a member of the InvaGen Pharmaceuticals Plant Quality Team. The position reports to the Manager of QA and may be matrixed to other functional leaders within the Quality or other departments. The essential and typically expected job duties for this position include but are not limited to the following:

• Perform in-process testing (e.g., weight, thickness, hardness, disintegration, friability, etc.) as per manufacturing batch record instructions.
• Conduct room and equipment checks (where applicable) prior to each stage of manufacturing by following detailed written procedures.
• Execute acceptable quality limit (AQL) sampling and inspections as required.
• Inspect in-process and finished product samples (where applicable) for the Quality Control (QC) Lab and follow detailed documentation procedures to deliver the results to the QC Lab.
• Maintain records of standard weights and perform daily verification of balances.
• Ensure the proper isolation of rejected material generated during batch process and accountability in the batch record.
• Monitor facility and product environmental operating conditions.
• Review engineering records such as temperature and humidity data calibration and PM records, pest control records, and contractor-related functions.
• Assess online batch records in terms of completeness of signatures, entries, and actual reconciliation/yields prior to initiation of the next processing step.
• Verify the functionality of all the equipment and associated controls during the batch run.
• Perform applicable testing and prepare reports for customer complaints.
• Identify and report any non-conformances and/or discrepancies to management if applicable.
• Complete other duties or participate in project work as assigned by management.

EDUCATION AND EXPERIENCE QUALIFICATIONS

• Minimum high school diploma.
• Advanced vocational training or education in pharmaceutical manufacturing, industrial management or related field of study from an accredited college/university is preferred.
• Minimum of three (3) years of experience in quality assurance in a GMP pharmaceutical manufacturing operation and work environment.
• Experience in MDI preferred.

KNOWLEDGE, SKILLS, AND ABILITIES

• Proficient user of personal computer hardware and software applications such as Microsoft Office tools, SAP, and other business applications.
• Must be able to influence decision-making and facilitate completion of work toward the achievement of the business plan and goals.
• Effective interpersonal relationship skills and the ability to work in a team environment.
• Proficiency in the English language to include usage, spelling, grammar, and punctuation.
• Must have current Good Manufacturing Practices (cGMP) knowledge.
• Must have strong attention to detail.
• Must be a self-starter and demonstrate initiative with seeking additional training or direction as needed.
• Must have strong organization and communication skills (written, verbal, and presentation).
• Must be detail-oriented with the ability to multitask and prioritize tasks with strict deadlines.

OTHER JOB INFORMATION

• No remote work available.