Biopharm Manufacturing Associates

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

Job summary

Alphanumeric Systems Inc is hiring Biopharm Manufacturing Associates in King of Prussia, PA. The role involves conducting GMP cleaning operations and ensuring compliance with safety requirements. Candidates should have a high school diploma and relevant experience in pharmaceutical cleaning operations.

Qualifications

• Minimum of 1 year experience in Sterile or GMP Cleaning.
• Familiar with cGMPs and regulatory guidelines.
• Strong communication skills, both verbal and written.

Responsibilities

• Follow all EHS procedures and report incidents promptly.
• Perform cleaning of production and lab areas.
• Maintain area cleanliness and adhere to cleaning schedules.

Skills

Communication

Cleansing techniques

Safety knowledge

GMP Compliance

Education

High School diploma or equivalent

Tools

SAP/MERPS

Microsoft Office

Job description

Alphanumeric is hiring Biopharm Manufacturing Associates to work in King of Prussia, PA, with a 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 shift work most likely from 12:00pm-12:00am, 3 or 4 times a week.

Qualifications:

• High School diploma or equivalent.
• 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 communication skills, both verbal and written.
• Basic knowledge and understanding of safety and GMP requirements.
• Proficiency in systems such as SAP/MERPS, VQD, Syncade, and Microsoft Office packages.
• Ensure proper procurement of materials for tasks.
• Ensure proper documentation of cleaning tasks.
• Strong focus on quality and compliance.

Key Responsibilities:

• Follow all EHS procedures, standards, and PPE requirements.
• Report incidents and accidents promptly.
• Raise ZAPs for EHS concerns.
• Participate in Safety Sessions.
• Follow GMP procedures.
• Report abnormalities or adverse events to FLL in a timely manner.
• Perform cleaning and recordkeeping per procedures.
• Adhere to cleaning schedules and maintain area cleanliness and tidiness.