GMP Cleaning Associate Job at Proclinical (King of Prussia)

Quality Lab Associate I

Conduct microbiological analysis, perform endotoxin and particulate matter testi...

Location

United States , Marion

Salary:

56000.00 - 77000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

B.S. degree in Microbiology, Biology, or related science
2-5 years of experience or Master’s Degree in biological sciences with 0-3 years experience, preferably in the pharmaceutical or medical device industry
computer literate/knowledge of Microsoft office applications (Word, Excel)
proficient in quality based computer systems such as LIMS, POMS, Endoscan-V software, Sampler Sight Pharma, and AS400
attention to detail and ability to prioritize multiple tasks
proficient in the operation of laboratory instrumentation and equipment such as laminar flow hoods, micro-pipettors, pH meters, analytical balances, and instruments used to perform particulate matter and endotoxin testing
good documentation skills and knowledge of GDPs (Good Documentation Practices)
knowledge of aseptic sampling and testing techniques and microbiological testing according to FDA, cGMP, GLPs and USP testing methodology
must be able to communicate effectively with supervisors and peers
must be experienced in executing general microbiology procedures

Job Responsibility

Prepare samples and perform endotoxin testing on raw materials, solution, and water for bioburden
perform particulate matter testing on solution
perform daily pH meter, balance, and pipette verification
perform daily Honeywell automated temperature checks and manual temperature monitoring
perform peptidoglycan and gel clot testing as needed
manage reagent inventory
generate monthly trend reports
calibration of micro-pipettes, analytical balance, water bath, dry heat bath, depyrogenation ovens, light obscuration particle counters and spectrophotometer
responsible for daily lab upkeep including cleaning, glassware washing and depyrogenation, supply replenishment, syringe and endotoxin prep
assist in method validation and protocol testing as needed

What we offer

Medical, Dental and Vision coverage
160 hours of Paid Time Off and Paid Holidays
401K match
Employee Stock Purchase Program
Paid Parental Leave
Tuition Reimbursement
short-term and long-term disability insurance
Employee Assistance Program
childcare benefits

Fulltime

Quality Control Technician

The Quality Control Technician reports to the Quality Manager. S/he is responsib...

Location

Canada , Hawkesbury

Salary:

Not provided

Biscuits Leclerc Ltd

Expiration Date

Until further notice

Requirements

Associates degree in Food Science and Technology, Biology, or equivalent combination of education/experience
Minimum of 2 years’ experience in technical field (engineering, food science, chemistry) with industry experience
Knowledge of GFSI / BRC, SQF, GMP and other food safety standard including HACCP or similar food industry regulations is preferred
Experience using Microsoft Office and other computer based applications (I pad, One Note, etc.)
Excellent people skills, maintain a positive attitude and ability to motivate people, specifically mentoring and coaching individuals
Ability to communicate effectively, both orally and written
Must be able read, interpret and comprehend weights, measurements, and mathematical equations
Be able to effectively understand and adhere to a variety of guidelines and work procedures (including health, safety, hygiene and sanitation), along with prioritizing and organizing workload
Ability to learn quickly and work both independently and as a team
Ability to work in a fast-paced, challenging, and consistently changing environment

Job Responsibility

Inspect the day-to-day quality and food safety activities
Effectively communicate quality control expectations to production personnel
Monitor GMP’s for compliance
Ensure that employees adhere to manufacturing, hygiene and sanitation standards
Conduct start-up and in-process checks to ensure the manufacturing process is conforming to customer specifications. This includes verification for correct product, correct formulation, documentation of ingredient lot numbers, correct code date / best by date etc.
May perform pre-operation inspection at the start of the production shift as well as pre- sanitation inspection at the end of the shift
Validate production pre-operational sheets are complete and accurate
Conduct metal detector and X-ray checks and monitoring through the course of the shift
Conduct sensory evaluations of raw materials and finished product, ensure specification compliance for finished products
Calibration of all scales and other laboratory equipment

What we offer

Working in a family business on a human scale
Evolving in a clean, temperate environment with the latest technology
Embracing high velocity production and cutting edge technology
Starting a new job with paid and adapted training
Earning a competitive salary
Benefiting from a complete benefits program (drug and dental insurance, 1 week of sick leave [conditions apply], telemedicine, group RRSP with employer participation and more)
Saving on our delicious products and discovering exclusive novelties
Taking advantage of job security and opportunities for advancement within the company
Integrating a rich company culture (Christmas, birthday and maternity gifts, use of the Poka platform and more)

Fulltime

Quality Control Technician

The Quality Control Technician reports to the Quality Manager. S/he is responsib...

Location

United States , Cornwall

Salary:

Not provided

Biscuits Leclerc Ltd

Expiration Date

Until further notice

Requirements

Associates degree in Food Science and Technology, Biology, or equivalent combination of education/experience
Minimum of 2 years’ experience in technical field (engineering, food science, chemistry) with industry experience
Knowledge of GFSI / BRC, SQF, GMP and other food safety standard including HACCP or similar food industry regulations is preferred
Experience using Microsoft Office and other computer based applications (I pad, One Note, etc.)
Excellent people skills, maintain a positive attitude and ability to motivate people, specifically mentoring and coaching individuals
Ability to communicate effectively, both orally and written
Must be able read, interpret and comprehend weights, measurements, and mathematical equations
Be able to effectively understand and adhere to a variety of guidelines and work procedures (including health, safety, hygiene and sanitation), along with prioritizing and organizing workload
Ability to learn quickly and work both independently and as a team
Ability to work in a fast-paced, challenging, and consistently changing environment

Job Responsibility

Inspect the day-to-day quality and food safety activities
Effectively communicate quality control expectations to production personnel
Monitor GMP’s for compliance
Ensure that employees adhere to manufacturing, hygiene and sanitation standards
Conduct start-up and in-process checks to ensure the manufacturing process is conforming to customer specifications. This includes verification for correct product, correct formulation, documentation of ingredient lot numbers, correct code date / best by date etc.
May perform pre-operation inspection at the start of the production shift as well as pre- sanitation inspection at the end of the shift
Validate production pre-operational sheets are complete and accurate
Conduct metal detector and X-ray checks and monitoring through the course of the shift
Conduct sensory evaluations of raw materials and finished product, ensure specification compliance for finished products
Calibration of all scales and other laboratory equipment

What we offer

Working in a family business
Evolving in a clean, temperate environment with the latest technology
Starting a new job with paid and adapted training
Benefit from a complete benefits program (drug and dental insurance, 1 week of sick leave [conditions apply], telemedicine, group RRSP with employer participation and more)
Save on our delicious products and discover exclusive novelties
Take advantage of job security and opportunities for advancement within the company
Integrate a rich company culture (Christmas, birthday and maternity gifts, use of the Poka platform and more)

Fulltime

Equipment Engineer

To conduct, coordinate and manage equipment related maintenance and improvement ...

Location

United Kingdom , Croydon

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Good level of experience of maintaining electrical and mechanical plant and equipment
A Craft Apprenticeship (& HNC preferred) in Electrical, Mechanical or Instrumentation Engineering
At least 5 years’ experience as a hands on multi-skilled engineer maintaining electrical, control, mechanical and pneumatic related plant and equipment
Experience of installation of new plant and equipment
Excellent interpersonal and communication skills
Responsive and flexible attitude to supporting internal and external customer requirements
Experience of working as a support function with a high focus on reliability
Rapid appreciation of issues, sound judgement and problem solving skills
Ability to work under pressure and to tight deadlines within a dedicated team
Knowledge and experience of clean room operations and associated equipment

Job Responsibility

Demonstrate a Safety first approach to every single aspect of the role
Lead trouble shooting, fault finding & resolution to root cause of compounding related plant and equipment
Lead shutdown planning and execution, inclusive of shutdown and start up activities
To implement the engineering improvement plan for the Compounding Unit
Heavy focus on reliability of plant and equipment, working relentlessly to ensure that plant availability & OEE metrics are continuously improved
To deliver best in class equipment availability and reliability through reactive, preventative and predictive maintence techniques
To plan and direct the installation, testing, operation, maintenance and repair of all facilities and equipment within the Compounding Unit
To develop and implement Preventative Maintenance procedures & schedules that assures equipment availability and reliability and product quality in line with the Compounding Engineering Strategy and Baxter Perfect Equipment requirements
Active member of the Perfect Equipment Steering Committee
Provide a standardised Perfect Equipment system across the Compounding Unit in collaboration with local operational staff and the UK Engineering Manager

What we offer

Competitive total compensation package
Professional development opportunities
High importance placed on work life balance
Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Fulltime

Equipment Engineer

Being an Engineer at Baxter means you play a critical role in helping us achieve...

Location

United Kingdom , Croydon

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Good level of experience of maintaining electrical and mechanical plant and equipment
A Craft Apprenticeship (& HNC preferred) in Electrical, Mechanical or Instrumentation Engineering is required
At least 5 years’ experience as a hands on multi-skilled engineer maintaining electrical, control, mechanical and pneumatic related plant and equipment
Experience of installation of new plant and equipment
Excellent interpersonal and communication skills
Responsive and flexible attitude to supporting internal and external customer requirements
Experience of working as a support function with a high focus on reliability
Rapid appreciation of issues, sound judgement and problem solving skills
Ability to work under pressure and to tight deadlines within a dedicated team
Knowledge and experience of clean room operations and associated equipment

Job Responsibility

Demonstrate a Safety first approach to every single aspect of the role
Lead trouble shooting, fault finding & resolution to root cause of compounding related plant and equipment
Lead shutdown planning and execution, inclusive of shutdown and start up activities
To implement the engineering improvement plan for the Compounding Unit
Heavy focus on reliability of plant and equipment, working relentlessly to ensure that plant availability & OEE metrics are continuously improved
To deliver best in class equipment availability and reliability through reactive, preventative and predictive maintence techniques
To plan and direct the installation, testing, operation, maintenance and repair of all facilities and equipment within the Compounding Unit
To develop and implement Preventative Maintenance procedures & schedules that assures equipment availability and reliability and product quality in line with the Compounding Engineering Strategy and Baxter Perfect Equipment requirements
Active member of the Perfect Equipment Steering Committee
Provide a standardised Perfect Equipment system across the Compounding Unit in collaboration with local operational staff and the UK Engineering Manager

What we offer

Competitive total compensation package
Professional development opportunities
High importance placed on work life balance
Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Fulltime

Quality Control Inspector

The QM Associate Scientist is required to perform testing of various Microorgani...

Location

United States , Sparks

Salary:

15.00 - 19.00 USD / Hour

MillenniumSoft Inc

Expiration Date

Until further notice

Requirements

Experience in handling biological or chemical samples and knowledge of GLP
Basic knowledge in a broad range of laboratory techniques
History of self motivation with a background in biological lab science
Demonstrated verbal and written communication skills in a team environment as well as a desire to work within a team
Capable of readily identifying and analyzing problems
Have basic analytical skills and be familiar with database and statistical software
BS or BA in related field required. Typical degree in Biological Sciences, Chemistry, Molecular, or related field

Job Responsibility

Responsible for Microbiology testing in peptone manufacturing, raw material products, and Final DCM testing as required
Perform testing of various Microorganisms in a Biosafety Level II / III Laboratory with strict adherence to safety policies
Ability to work in a clean room environment and meet validation requirements associated with donning and doffing clean room garments
Responsible for Microbiology testing of prepared media as well as preparing various medias from scratch

Fulltime

Senior Administrator

At STERIS, we help our Customers create a healthier and safer world by providing...

Location

Ireland , Westport

Salary:

Not provided

STERIS

Expiration Date

Until further notice

Requirements

Outgoing, pleasant personality, Good communication skills
Reception and telephone-answering techniques
Initiative, ability to take responsibility and to work without direct supervision or instruction
Achieve error free output to customers
Provide expedient and appropriate response to customer inquiries
Maintain archive files of all quality records
Understand the documentation system and ensure that it is operated correctly
Proficient with MS Office suite

Job Responsibility

Perform defined secretarial and administrative duties to support the plant team, to maintain records and to manage office administration
Project a positive image of the organisation
create a positive working environment and will lead continuous improvement initiatives with Steris Westport Site
Assist visitors and telephone callers by making them welcome and taking care of their needs in a timely, efficient and friendly manner
Maintain up-to-date and efficient filing system of all process records and other administration documents
Provide secretarial support including maintaining archives, stationary management, scheduling meetings, etc
Prepare purchase requisitions and purchase orders, manage receipts and provide administration for all associated accounting
Reinforce impression of a quality GMP Healthcare company by maintaining reception and public areas clean and tidy
Undertake other duties, tasks and responsibilities as may be assigned by the Management from time to time
To ensure compliance with safety procedures at all times

Manufacturing Associate, Pilot Plant - Upstream

Amgen is seeking an entry‑level Associate to implement a variety of production a...

Location

United States , Thousand Oaks

Salary:

75618.00 - 89473.00 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

High school diploma / GED and 2 years of Manufacturing, Scientific or Operations experience
Associate’s degree and 6 months of Manufacturing, Scientific or Operations experience
Bachelor’s degree
Strong verbal and written communication skills
Demonstrated analytical, project management, and continuous improvement abilities
Experience working in GMP / GDP‑regulated environments
Ability to work off‑hours or alternative shifts

Job Responsibility

Perform hands‑on operation of current and future cell culture equipment, including Wave bioreactors, Stainless steel and single‑use bioreactors, ATFs and associated equipment cleaning
Support pilot‑scale upstream processes from scale‑up through harvest
Execute production runs, experiments, and technology development activities
Support new product introductions (NPI) and technology transfer
Participate in equipment commissioning and equipment design
Design experiments and analyze process data
Document work through Standard Operating Procedures (SOPs), Electronic lab notebooks, Manufacturing procedures, Presentations or meeting notes
Summarize findings, identify process challenges, and support future commercial process development

What we offer

A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
A discretionary annual bonus program
Stock-based long-term incentives
Award-winning time-off plans

Fulltime

GMP Cleaning Associate

Proclinical

Location:
United States , King of Prussia

Category:
Manufacturing

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
February 19, 2026

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Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:February 19, 2026

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