Pharmaceutical Production Operator

Linked Professional Services; Piscataway Township (NJ); Vor Ort; USD 55.000 - 75.000; Vollzeit

Benefits dieser Stelle

Medical Insurance

Vision Insurance

401(k)

Zusammenfassung

Linked, LLC is seeking an experienced Pharmaceutical Production Operator for Granulation, Compression, and Coating operations in a fast-paced, regulated environment. This role requires solid oral dosage manufacturing experience and strict adherence to cGMP standards.

You will operate and monitor equipment, follow BMRs and SOPs, document production activity, and collaborate with QA and maintenance. Overtime and Saturdays may be required.

Qualifikationen

• 3–5+ years of hands-on pharmaceutical manufacturing experience.
• Direct experience in solid oral dosage production essential.
• Experience with Granulation, Compression, and Coating equipment.
• Familiar with cGMP, SOPs, and BMRs.
• Ability to work overtime and Saturdays if needed.

Aufgaben

• Operate, monitor, set up, and clean Granulation, Compression, and Coating equipment.
• Perform daily manufacturing operations per cGMP and SOPs.
• Follow Batch Manufacturing Records (BMRs) to ensure accuracy.
• Monitor equipment performance and maintain product quality.
• Identify deviations, document issues, and report promptly.
• Perform line clearance, cleaning, and changeover between batches.
• Maintain accurate production documentation and records.
• Adhere to FDA regulations and safety standards.
• Collaborate with production, QA, and maintenance teams.
• Maintain a clean, compliant production environment.

Kenntnisse

Granulation

Compression

Coating

Solid dosage

cGMP

SOPs

BMRs

FDA regulations

Quality documentation

Team collaboration

Jobbeschreibung

Pharmaceutical Production Operator – Granulation, Compression & Coating
Shift: 1st Shift | 7:00 AM – 3:00 PM
Schedule: Monday – Friday | Potential Overtime and Saturdays
Experience Required: 3–5+ Years of Pharmaceutical Manufacturing Experience
Industry: Pharmaceutical Manufacturing
Type: Contract-to-hire

Position Overview

We are seeking experienced Pharmaceutical Production Operators with a strong background in solid oral dosage manufacturing, specifically Granulation, Compression, and Coating processes. This position involves operating specialized pharmaceutical manufacturing equipment while ensuring compliance with FDA regulations, current Good Manufacturing Practices (cGMP), and established quality standards.

The ideal candidate will have 3–5+ years of direct pharmaceutical production experience and be comfortable working in a fast-paced, highly regulated manufacturing environment.

Key Responsibilities

• Operate, monitor, set up, and clean pharmaceutical manufacturing equipment used in Granulation, Compression, and Coating processes.
• Perform daily manufacturing operations in accordance with cGMP guidelines and established Standard Operating Procedures (SOPs).
• Follow Batch Manufacturing Records (BMRs) to ensure accurate and consistent production processes.
• Monitor equipment performance and manufacturing processes to maintain product quality and efficiency.
• Identify, document, and report process deviations, equipment malfunctions, and quality concerns.
• Perform equipment cleaning, line clearance, and changeover activities between production batches.
• Maintain accurate production documentation and manufacturing records.
• Follow all FDA regulations, safety procedures, and pharmaceutical quality standards.
• Collaborate with production, quality assurance, and maintenance teams to resolve manufacturing issues.
• Maintain a clean, organized, and compliant production environment.

Required Qualifications

• Minimum 3–5 years of hands-on pharmaceutical manufacturing experience required.
• Direct experience in solid oral dosage manufacturing is required.
• Experience operating pharmaceutical Granulation, Compression, and/or Coating equipment.
• Strong understanding of cGMP regulations and pharmaceutical manufacturing procedures.
• Experience following SOPs and completing Batch Manufacturing Records (BMRs).
• Ability to operate, monitor, and clean pharmaceutical production equipment.
• Ability to identify manufacturing deviations and maintain strict quality standards.
• Strong attention to detail, documentation accuracy, and workplace safety.
• Ability to work independently and collaboratively in a team-oriented manufacturing environment.
• Flexibility to work overtime and Saturdays as needed.
• Medical Insurance
• Vision Insurance
• 401(k)

Previous hands-on pharmaceutical production operator experience is mandatory. Candidates must have direct experience in regulated pharmaceutical manufacturing, preferably involving solid oral dosage processes such as Granulation, Compression, or Coating. General manufacturing experience alone does not meet the requirements for this position.

Pharmaceutical Production Operator – Granulation, Compression & Coating
Shift: 1st Shift | 7:00 AM – 3:00 PM
Schedule: Monday – Friday | Potential Overtime and Saturdays
Experience Required: 3–5+ Years of Pharmaceutical Manufacturing Experience
Industry: Pharmaceutical Manufacturing
Type: Contract-to-hire

Position Overview

We are seeking experienced Pharmaceutical Production Operators with a strong background in solid oral dosage manufacturing, specifically Granulation, Compression, and Coating processes. This position involves operating specialized pharmaceutical manufacturing equipment while ensuring compliance with FDA regulations, current Good Manufacturing Practices (cGMP), and established quality standards.

The ideal candidate will have 3–5+ years of direct pharmaceutical production experience and be comfortable working in a fast-paced, highly regulated manufacturing environment.

Key Responsibilities

• Operate, monitor, set up, and clean pharmaceutical manufacturing equipment used in Granulation, Compression, and Coating processes.
• Perform daily manufacturing operations in accordance with cGMP guidelines and established Standard Operating Procedures (SOPs).
• Follow Batch Manufacturing Records (BMRs) to ensure accurate and consistent production processes.
• Monitor equipment performance and manufacturing processes to maintain product quality and efficiency.
• Identify, document, and report process deviations, equipment malfunctions, and quality concerns.
• Perform equipment cleaning, line clearance, and changeover activities between production batches.
• Maintain accurate production documentation and manufacturing records.
• Follow all FDA regulations, safety procedures, and pharmaceutical quality standards.
• Collaborate with production, quality assurance, and maintenance teams to resolve manufacturing issues.
• Maintain a clean, organized, and compliant production environment.

Required Qualifications

• Minimum 3–5 years of hands-on pharmaceutical manufacturing experience required.
• Direct experience in solid oral dosage manufacturing is required.
• Experience operating pharmaceutical Granulation, Compression, and/or Coating equipment.
• Strong understanding of cGMP regulations and pharmaceutical manufacturing procedures.
• Experience following SOPs and completing Batch Manufacturing Records (BMRs).
• Ability to operate, monitor, and clean pharmaceutical production equipment.
• Ability to identify manufacturing deviations and maintain strict quality standards.
• Strong attention to detail, documentation accuracy, and workplace safety.
• Ability to work independently and collaboratively in a team-oriented manufacturing environment.
• Flexibility to work overtime and Saturdays as needed.
• Medical Insurance
• Vision Insurance
• 401(k)

Benefits

• Medical Insurance
• Dental Insurance
• Vision Insurance
• 401(k)

Important Experience Requirement

Previous hands-on pharmaceutical production operator experience is mandatory. Candidates must have direct experience in regulated pharmaceutical manufacturing, preferably involving solid oral dosage processes such as Granulation, Compression, or Coating. General manufacturing experience alone does not meet the requirements for this position.

Linked, LLC is an equal opportunity employer committed to creating a diverse and inclusive workplace. We celebrate and embrace differences and are dedicated to providing equal employment opportunities to all individuals regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or veteran status. Our goal is to ensure that every employee and applicant is treated with respect and fairness. We welcome and encourage applications from all qualified candidates and are committed to making reasonable accommodations to support diverse needs throughout the hiring process. Linked, LLC is proud to be an equal opportunity employer and is dedicated to fostering a work environment where everyone can thrive.