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Drug Product Manufacturing Technician I/II/III - 2nd Shift

PCI Pharma Services · Madison, WI

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Level
Technician
Team
Manufacturing
Experience asked
2+ years
Industry
Pharma & life sciences
Posted
Yesterday

The role in 30 seconds

An engineer-level manufacturing role at PCI Pharma Services (pharma & life sciences) in Madison, WI.

They ask for
2+ years
Tools it names
FDA / GMP, Validation (IQ/OQ/PQ)

Read from the posting. The full description is below.

How this role compares

Against 16 other live manufacturing postings in Wisconsin.

Experience asked
Less than usual (2+ vs 4+)

Similar roles usually ask 4+ years.

Skills these teams ask for most

  • ✓ Team leadership 59%
  • CNC 53%
  • Machining 53%
  • Tooling 47%
  • Robotics 29%
  • GD&T 29%

✓ = this posting asks for it too. % = share of similar postings that mention it.

It asks for 2+ years. If you're close, apply anyway: requirements are a wish list. Talk to someone on the team first.

At a glance

Pulled from the posting text. If it's not listed here, the posting didn't say.

How to get in at this plant

Five moves over a week or two. The first one takes ten minutes.

  1. 1

    Pick 2–3 people on the Manufacturing team at PCI Pharma Services

    We found 1 person at this company and state: 1 on the team. Engineers who joined in the last year or two reply the most. See them ↓

  2. 2

    Send a short, curious note

    One real question about their work. No favors yet. Each person gets a different note, written for this role.

    Write to Jason → (free)
  3. 3

    Turn a reply into a short call

    Questions worth asking about this team:

    • What does a normal week look like on your team?
    • Is the work mostly new product launches or sustaining existing lines?
    • How much time do you spend on the floor versus at a desk?
    • How did you land the job? What stood out in your interviews?
  4. 4

    Apply with someone vouching for you

    If the call went well, ask whether they’d pass your résumé to the hiring manager. Send your résumé link, apply that day, and let them know.

  5. 5

    Bring proof to the interview

    One page of before-and-after numbers from projects you led: scrap, OEE, cycle time, cost. Plant managers hire on results.

This plant: PCI Pharma Services in Madison

6 other open roles at this site · 1 person we found on the manufacturing team.

Full description from PCI Pharma ServicesAs posted on their careers site.Show

Responsibilities

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The essential duties and

responsibilities

include the following but other duties may be assigned.

  • ◆Maintains and adheres to safe work habits and all applicable PCI safety procedures and guidelines.
  • ◆Demonstrates general knowledge of aseptic techniques.
  • ◆Prepares solutions, aseptic filling, and labeling of vials under sterile and non-sterile conditions, routine solution and filtration, vial and component preparation and sterilization.
  • ◆Assembles, disassembles, and operates aseptic filling equipment and lyophilizer equipment in classified cleanroom and controlled non classified environments. Operates vial capper, unloads product from lyophilizers and liquid fill line.
  • ◆Prepares equipment and components for sterilization and Lyophilization.
  • ◆Operates processing equipment including autoclaves, ovens, vial washers, and depyrogenation, centrifuges, mills equipment.
  • ◆Assists in the formulation and dispensing of product in a clean room environment per SOPs and MBRs
  • ◆Sanitizes production areas and prepares equipment for production.
  • ◆Completes and maintain documentation related to assigned work, including logbooks, batch records, etc.
  • ◆Adheres to verbal instructions and written procedures in operating production equipment and performing processing steps; accurately completes appropriate production documentation.
  • ◆Identifies, escalates and documents events that deviate from normal operation; participate as needed in investigations.
  • ◆Maintains compliance, cleanliness and orderliness of operational areas per appropriate SOPs.
  • ◆Performs COP, CIP, and SIP operations to prepare equipment for manufacturing operations.
  • ◆Reviews and revises pertinent SOPs and production batch records as required.
  • ◆Inspire and constantly strive to make PCI a great place to work and respected for the quality of its people and products and clients.
  • ◆Successfully participates in media fill/aseptic proficiency test

Special Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. The employee must be physically capable to perform the duties listed below with or without reasonable accommodations which may be made to enable individuals with disabilities to perform the essential functions.

  • ◆Ability to wear personal protective equipment such as safety glasses/goggles, gloves, and safety shoes.
  • ◆Ability to gown and gain entry to controlled manufacturing areas.
  • ◆Ability to lift, pull or push equipment requiring up to 25-50 lbs of force.
  • ◆Ability to stand for 6 hours in a production suite.
  • ◆Ability to work any shift (up to 10 hours) as required dependent on business needs.

Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

  • ◆Interacts with cross functional support teams such as Operations, QA, QC, Engineering, R&D, Validation, etc.
  • ◆This is an individual contributor role.
  • ◆Ability to adapt to a changing process daily (i.e., Formulations vary depending on client product)
  • ◆Able to work under the scrutiny of clients daily
  • ◆Expected to be flexible with the process and adjust work hours accordingly

Qualifications

The

requirements

listed below are representative of the knowledge, skill, and/or ability required for the stated position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

  • ✓0 – 2+ years of working experience, preferably in a manufacturing environment ideally in the pharmaceutical or medical device industry.
  • ✓Minimum of a High school diploma/equivalency.
  • ✓Ability to weigh and measure raw materials and operate basic Benchtop instruments.
  • ✓Able to follow written instructions. Seeks help with more complex and non-routine tasks.
  • ✓Ability to adapt to a changing process daily (i.e., Formulations vary depending on client product)
  • ✓Able to work under the scrutiny of clients daily
  • ✓Expected to be flexible with the process and adjust work hours accordingly
  • ✓Good verbal and written skills
  • ✓Pay attention to detail. Demonstrates a good mechanical aptitude.
  • ✓Commits to conducting PCI business according to the highest legal and ethical standards, and to continually pursue excellence in the manufacturing and delivery of PCI products and services.
  • ✓Honesty, integrity, respect and courtesy with leadership and peers
  • ✓Openly receives and implements feedback, resilient, able to move p
Show full description ↓

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.

We are PCI.

Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.

The Manufacturing Technician learns and performs a variety of tasks with supervision and in accordance with the manufacturing instruction set inclusive of current GMP/ISO requirement and standards and following all safety guidelines of PCI. With supervision, the technician performs routine and critical manufacturing operations, including but not limited to work functions in equipment prep, formulation, aseptic compounding, and filling activities for biopharma and medical device products. Works with Master production records and standard operating procedures. Conducts self in accordance with the Guardian values and behaviors.

Schedule

Will train on first shift and then moved to a designated 2nd shift: M-F 4:00PM to 12:30AM

Eligible for 10% pay differential when working 2nd shift hours

Looking to hire various levels based on experience.

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