Manufacturing Associate Biopharm King of Prussia PA

Alphanumeric Systems; King of Prussia (Montgomery County); On-site; USD 60,000 - 80,000; Full time

Job summary

A leading company in the pharmaceutical sector is hiring Biopharm Manufacturing Associates in King of Prussia, PA. The role involves cleaning and maintaining production areas in line with high safety and quality standards, necessitating experience in GMP operations. Off-shift hours may be required for this 1-year contract position.

Qualifications

• 1 year experience in Sterile or GMP Cleaning operations or 5 years equivalent experience.
• Familiar with cGMPs, regulatory guidelines, and standard operating procedures.
• Prior experience with pharmaceutical manufacturing preferred.

Responsibilities

• Follow all EHS procedures and notify personnel of any incidents.
• Perform area cleaning and maintain 5S standards.
• Adhere to GMP procedures and site cleaning protocols.

Skills

Strong communications skills

Basic knowledge of safety and GMP requirements

Quality/compliance orientation

Education

High School

Tools

SAP/MERPS

VQD

Syncade

Microsoft software packages

Job description

Alphanumeric is hiring Biopharm Manufacturing Associates to work in King of Prussia, PA with our client of 20 years committed to improving lives through medical and pharmaceutical advancements.

Main objective is to clean the production, lab, and warehouse areas according to site procedures and comply with safety and quality requirements. Conduct GMP Cleaning operations in accordance with Biopharm Safety Procedures and cGMPs. Off-shift hours (including night work) may be required.

This role requires full eligibility to work in the USA. We do not offer work visa sponsorships for this position.

CONDITIONS :

• Type of employment : W2 Contract (on-site). MUST BE ABLE TO WORK ON A W2
• Pay rate : 22.50$/hour
• Duration : 1 year
• Work location : King of Prussia, PA
• Working hours : First couple of weeks 7:30am-4:00pm for training. Then do shift work most likely from 12:00pm-12:00am, 3 or 4 times a week.

Qualifications :

• High School
• Minimum of 1 year experience in Sterile or GMP Cleaning operations within Pharmaceutical or Biotechnology industry or 5 or more years of equivalent experience
• Prior experience with pharmaceutical manufacturing
• Familiar with cGMPs, regulatory guidelines, governmental codes, and standard operating procedures.
• Strong communications skills, both verbal and written.
• Basic knowledge and understanding of safety and GMP requirements.
• Demonstrates proficiency on the following systems: SAP/MERPS, VQD, Syncade, Microsoft software packages.
• Ensure the proper procurement of appropriate materials for tasks.
• Ensure proper documentation is completed appropriately to sufficiently document cleaning tasks.
• Strong quality/compliance orientation and track record.

Key Responsibilities:

• Follow all EHS procedures, standards and PPE requirements

• Notify appropriate personnel of any incident and accident in the respective area.

• Raise ZAPs for any EHS concerns.

• Attended Stop for Safety Sessions in respective shift/area

• Follow GMP procedures.

• Report any abnormalities /adverse event to FLL (OLN, Rapid Response, deviation) in a timely manner.

• Perform area cleaning and record per procedure.

• Adhere to the site cleaning procedure and schedule

• Maintain 5S, area cleanness and tidiness.