Process Operator

ZipRecruiter; Malvern; On-site; GBP 20,000 - 30,000; Full time

Job summary

A leading company in pharmaceutical manufacturing is seeking a Process Operator for a temp-to-hire position. The role involves micronization and milling of pharmaceutical ingredients following cGMP guidelines. Candidates must have a High School Diploma or GED and prior experience in a regulated environment is preferred. Excellent communication and basic math skills are essential, along with the ability to adhere to safety and quality standards. This position offers an opportunity to develop skills in a fast-paced production setting.

Qualifications

• Dependable and eager to learn, able to meet job's physical requirements.
• Prior manufacturing experience in a regulated environment preferred.

Responsibilities

• Perform entry-level micronization and milling of pharmaceutical materials.
• Adhere to safety and quality procedures in all operations.
• Document production activities accurately following standards.

Skills

Communication Skills Oral and Written

Basic Math Skills

Education

High School Diploma or GED

Tools

Personal Protective Equipment

Job description

Job DescriptionJob DescriptionImportant Notice: Protecting Your Information
Medvacon Talent Acquisition only conducts initial video interviews via Microsoft Teams or Zoom. All communication will come from an email address ending [e-mail]. If you receive a message that seems suspicious or is not from our official domain, please report it immediately [e-mail].

This is a temp-to-hire 1099 position with no benefits.

Shift: 1PM-11:30PM

The Process Operator micronize\mills client provided material including both active pharmaceutical ingredients and excipients as per Client procedures and policies, instructions and cGMP guidelines. Consistently models values and leadership behaviors in all interactions.

• Perform entry-level micronization and milling of both hazardous and non-hazardous pharmaceutical actives and excipients.
• Set up, operate equipment, and monitor production processes.
• Report production on batch records following good documentation procedures (GDPs).
• Work in a regulated environment with adherence to standard operating procedures and policies.
• Adhere to cGMP standards.
• Identify and communicate non-routine events, deviations, and GMP deficiencies to supervisor promptly.
• Clean the entire processing area and processing equipment.
• Produce thorough, clear, and consistent documentation in compliance with Quality Standards (Attributable, Legible, Contemporaneous, Original, and Accurate).
• Demonstrate willingness to accept change, learn, and work with new processes.
• Stop and ask questions or suggest improvements when something is unclear.
• Participate in shift change meetings, site/team meetings, sending/receiving emails, offering suggestions for improvements, and participating in projects.
• This is a site-based position.
• Strive to achieve First Time Right (FTR) as a key performance indicator (KPI) in order to meet our yearly targets.
• Remain current with Compliance Wire and other site training.
• Perform all other duties assigned by management

Measures of Performance:

• Adherence to safety and quality procedures
• Product quality, throughput and final yields
• Excellent attendance, punctuality, and dependability
• Operators’ work ethic and general attitude as it pertains to the daily operations of the facility

II. Position Requirements:
Education or Equivalent: High School Diploma or GED

Experience:

• Must be dependable, ready/eager to learn and able to meet the physical requirements of the job.
• Prior manufacturing experience and work in a regulated environment .
• Ability to work weekday and weekend OT a plus.

Knowledge/Skills Requirements: Technical Skills/Knowledge

• Communication Skills Oral and Written
• Basic Math Skills, interpretation
• Potential limited exposure to heath & physically hazardous chemicals.
• Personal protective equipment, including gloves, a respirator hood, safety glasses, safety shoes and other Personal Protective Equipment is provided and is required to be worn in designated areas.
• Prior Production Experience

Physical Requirements/Work Environment:

• Physical strength, stamina and dexterity while wearing fully enclosed air suite
• Employees be able to lift or move items up to 44 lbs. (20kg) individually, or with a two-person lift between 45 lbs and 76 lbs. (35kg). 77 lbs and over with a lift assistance device.
• Ability to work safely with high potency active pharmaceutical ingredients (HPAPI) as well as novel compounds of unknown potency and toxicity
• Ability to perform moderate physical labor

Important Notice: Protecting Your Information
Medvacon Talent Acquisition only conducts initial video interviews via Microsoft Teams or Zoom. All communication will come from an email address ending in @medvacon.com. If you receive a message that seems suspicious or is not from our official domain, please report it immediately to [e-mail].

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