Experienced pharmaceutical operator Job at Randstad (Mississauga)

Quality Assurance Technician

Ensure and assist with site-specific quality compliance according to Strive Phar...

Location

United States , Leesburg

Salary:

Not provided

Strive Compounding Pharmacy

Expiration Date

Until further notice

Requirements

Minimum of High School Diploma/GED with work experience
Minimum of 2 years experience in a quality or manufacturing department of a Pharmaceutical, Medical Device, or Allied Health Science
Experienced in aseptic operations
Experience within a regulated environment
Knowledge & skills in Pharmaceutical Quality Assurance Practices
Associates Degree or higher level degree in technician technical scientific discipline
Biology, Microbiology, Chemistry, or Pharmacy
Strong organizational skills and attention to detail
Ability to effectively troubleshoot issues
Comfortable working in a cleanroom-working environment that may be limited to a small area, wearing protective cleanroom attire, tolerating controlled temperatures, and loud noise

Job Responsibility

Perform product inspection for defects, leaks, and particulates
Environmental monitoring of personnel (as needed) and complete documentation
Assist in the media fill process validations to include inspection of filled units
Perform documentation review of compounding activities such as cleaning records, line clearance forms, and inventory sheets
Verify that raw materials meet specification
Account for labeling
Review temperature and BMS alarms
Ensure that product test results meet specification limits
Checking that all documentation is complete
Document non-compliance and work with supervisor/lead if further investigation is needed appropriate lab for particulate identification or microbial analysis

What we offer

Employer paid healthcare coverage available after 30 days of employment
Choice of an FSA/HSA
Voucher for new hire scrubs (if applicable)
Parental leave
401(k) plan with matching contributions
Weekends and holidays off
FREE COMPOUNDED MEDS to employees and immediate family members

Fulltime

Head of Training and Compliance - Aseptic Services

Leadership role to lead strategic direction of training governance, regulatory a...

Location

Salary:

Not provided

360 Resourcing Solutions

Expiration Date

Until further notice

Requirements

Passionate & Driven
Experienced in a similar role and can operate autonomously
Collaborative team player
Experienced in Pharmaceutical/Healthcare with background in GMP Aseptic pharmaceutical or healthcare
Strong Communication Skills
Tech-Savvy and highly proficient with all Microsoft Office software

Job Responsibility

Development and Implementation of training strategies across all manufacturing sites
Developing and monitoring metrics for training compliance and effectiveness
Ensuring all new starters have a great joining experience
Supporting work based apprentice and students placement supervisors
Participate in promoting training and education both internally and externally
Committing to ongoing CPD and attending courses
Developing and leading a high functioning site-based training team
Ensure appropriate level of resource and expertise is in place
Ensure team have clear objectives in place

What we offer

Career Progression and professional development opportunities
Pension & Benefits including a cycle-to-work scheme
Free Food & Drinks
Vibrant Work Culture with regular events organised by Social Committee

Process Development Senior Engineer

Process Development Senior Engineer for Amgen Singapore Manufacturing. Amgen is ...

Location

Singapore , Tuas

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree
Master’s degree and 2 years of directly related experience
Bachelor’s degree and 4 years of directly related experience
Diploma and 8 years of directly related experience
6+ years of relevant work experience in the commercial manufacturing environment within the biotechnology or pharmaceutical industries
At least 4 years’ experience with regulated environments (i.e. cGMP) required
In depth cell culture and/or purification process knowledge, including single-use technologies and harvest technologies
Good understanding of process characterization and process scale up to resolve technical issues observed during transfer / manufacturing at large scale.
Experienced in providing floor support, troubleshooting unit operations, and resolving and documenting investigations to support cGMP production
Experienced in Technology Transfer of new process and technology to commercial site.

Job Responsibility

Assume a Subject Matter Expert role within ASM Process Development for cell culture and/or purification commercial process support.
Act as Drug Substance Team Leader within the global Product Development Team (PDT)
providing stewardship of product lifecycle and process improvement.
Lead complicated investigations independently, providing concise communications to teams and leadership
Integrate trends, data and information into plans, deliverables and recommendations
Manage key projects to deliver site goals while meeting quality, schedule, and cost objectives.
lead productivity projects, process optimization, and product life cycle management.
Collaborate with cross-functional teams and network drug substance teams to resolve process challenges by applying advanced technical principles and concepts for troubleshooting.
Apply best practices to leverage data for more proactive and predictive approaches.
Support regulatory filings, audits and inspection, and other CMC activities (e.g author and review regulatory submissions and responses to questions as required).

What we offer

Vast opportunities to learn and move up and across our global organization
Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

Account Strategist

Creative, mission-focused, fast-paced health sciences marketing agency seeks a f...

Location

United States , Kearney; Omaha

Salary:

Not provided

SCORR Marketing

Expiration Date

Until further notice

Requirements

5-7 years of related work experience in advertising, marketing, or B2B marketing with a full-service agency, preferably with a focus in life science, health care, or pharmaceuticals
Experienced B2B marketer, skilled at developing holistic, omni-channel integrated marketing plans as well as developing, driving, and deploying strategy
Able to work in a fast-paced, quality and results focused environment
Must be able to simultaneously focus on big picture, details, and driving results
Strategic and growth mindset paired with exceptional critical-thinking skills
Solution oriented
Proactive and thorough communicator, both verbal and written

Job Responsibility

Operate as the lead client point of contact for all matters specific to your accounts and serve as the liaison between SCORR’s clients and internal teams
Partner with your Project Manager to ensure the timely and successful delivery of each initiative according to customer needs and strategic objectives – on time, on budget, and on strategy
Work with client and internal teams on the execution of all marketing tactics including, but not limited to, branding, market intelligence, video, digital/media, PR/communications, trade shows, sales enablement, etc.
Comfortable working with individuals in all levels of the client organization, including strong skills interacting with C-suite and senior-level management
Contribute to organic sales growth with existing clients
Understand and keep up to date with industry and competitive landscape knowledge

Fulltime

Senior Director, Analytical Development and Quality Control

The Altos Institute of Medicine will capture knowledge generated about cell heal...

Location

United States , Redwood City

Salary:

283900.00 - 384100.00 USD / Year

Altos Labs

Expiration Date

Until further notice

Requirements

Ph.D. in analytical sciences or biological sciences
Minimum 15+ years of analytical development and QC experience in biotech/pharmaceutical industry
10+ years of Management experience
Highly experienced in developing and implementing assays for Quality Control testing and characterization of drug substance, drug product and manufacturing in-process samples
Experienced in multiple modalities including biologics, oligonucleotides, small molecules, mRNA/LNP and AAV gene therapy
Experienced in leading CMC team and analytical subteam
Proficient in cGMP’s and pharmaceutical industry procedures and regulations
Highly experienced in achieving CMC deliverables through outsourcing to Contract Manufacturing Organizations
Leadership experience in managing diverse project activities with contract CDMO facilities at global locations
A critical thinker with the ability to analyze possibilities and solutions and make pragmatic trade-offs

Job Responsibility

Lead analytical development and quality control across multiple modalities
Build a high performing team and establish internal and external analytical and QC capabilities
Serve as CMC lead and analytical lead for Altos therapeutic programs
Manage contract manufacturing organizations and CROs to develop and qualify analytical testing methods, perform product characterization, release and stability testing, and in-process testing
Establish product specifications to ensure product quality
Support technical assessment of Out of Specification and Non-Conforming investigations
Author, review, and/or approve Standard Operating Procedures, specifications, regulatory filing, or other controlled documents
As a member of the Tech Ops leadership team, build the Tech Ops organization, processes, systems and infrastructure
Create and foster strong partnerships with Institutes of Science, Institutes of Technology, Institute of Computation, drug discovery and development sciences, clinical, regulatory, program management, business development, legal and finance
Actively contribute to a team culture that promotes continuous improvement, accountability, professional growth, and inclusion

Fulltime

Maintenance Mechanic II

Life changing therapies. Global impact. Bridge to thousands of biopharma compani...

Location

Canada , Mississauga

Salary:

32.23 - 36.26 CAD / Hour

PCI Pharma Services

Expiration Date

Until further notice

Requirements

MUST HAVE a License Industrial Mechanic Millwright (433A)
6 to 10 years of working experience exclusively as a technician in a pharmaceutical packaging environment
Experienced Licensed Industrial or Construction and Maintenance Electrician (442A or 309A), with strong electrical and technical aptitude and/ or 6 to 10 years of working experience
None licensed candidates must complete and pass a technical aptitude test involving hands-on demonstration
General technical knowledge and experience concerning electrical, pneumatic, and HVAC
Core skills in Mathematics and English usually associated with grade 12
Interpersonal skills to work co-operatively with Line Leaders, Packagers, and Project Coordinators/Managers

Job Responsibility

Set-up and operation of machinery used in the packaging of pharmaceutical products (e.g. Cartoning, Blistering and bottling equipment, inkjet coder, checkweigher, etc.)
Disassembles and cleans all change parts/production room as outlined in SOP's
Responsible for the operation of the Line from a production standpoint partnering with QA, Maintenance Trades, Packagers and Line Leaders
Reads and understands packaging procedures prior to each job
Adheres to standard SOP's and job specific packaging procedures
Troubleshoots setup, equipment and facility issues and uses trigger points to escalate for support to ensure production runs are executed efficiently, with high quality and minimal waste
Performs in-process checks and inspections
Partners with the Maintenance Trades to troubleshoot electrical/mechanical problems and repairs
Performs packaging tasks associated with packaging pharmaceutical product
Assists in the orientation and training of new Packagers and Maintenance personnel on duties to be performed

What we offer

Paid time off
Extended health benefits (including dental and vision)
Life and disability insurance
Retirement savings options such as an RRSP with employer contributions
Additional wellness and employee-support programs may also be available
Eligibility for an annual performance bonus

Fulltime

New

Senior Critical Environment Technician- Controls SME

As a Senior Critical Environment Technician (CET) - Controls SME in Microsoft’s ...

Location

United States , Phoenix

Salary:

33.46 - 55.67 USD / Hour

Microsoft Corporation

Expiration Date

Until further notice

Requirements

High School Diploma, GED, or equivalent
3+ years mission critical services work/applied learning experience (e.g., high availability assembly/manufacturing/critical infrastructure environments such as data centers, oil and gas refineries, hospitals, pharmaceutical, manufacturing, or related fields) OR equivalent experience
1+ year(s) experience in a specialized area (e.g., mechanical field, electrical field, controls field) or related field
Ability to meet Microsoft, customer and/or government security screening requirements are required for this role
Ability to meet Microsoft Cloud background check upon hire/transfer and every two years thereafter

Job Responsibility

Understands, follows, and ensures safety and security requirements (e.g., job hazard assessments [JHAs], toolbox talks), and business processes and procedures are met, to properly perform work in a safe, quality, and reliable manner in accordance to applicable Authority Having Jurisdiction (AHJ) regulations, and Microsoft requirements
Processes method statement of work (MSOW) documents
Coordinates activities and associated schedules with contractors
Performs inspections of equipment in a facility
Participates in testing and commissioning activities
Advises engineer partners or project management colleagues on project scope process or execution methodology
Presents for review and approval MSOW in their area of responsibility
Prepares and submits highly complex reports as assigned following preexisting scripts and templates, or using ad hoc methods required to support trending and analysis (e.g., Root Cause Analysis [RCA] reports) and may review prior reports delivered by less experienced team members
Develops methods of operating procedure (MOPs), standard operating procedures (SOPs), and/or digital methods of operating procedures (DMOPs) for highly complex and/or interdependent equipment and disciplines to ensure safe and reliable execution
Reviews completed work using approved tools and procedural templates from less experienced technicians for accuracy and completeness

Fulltime

Senior Critical Environment Technician - Night Shift

As a Senior Critical Environment Technician (CET) - Night Shift in Microsoft’s C...

Location

United States , Goodyear

Salary:

33.46 - 55.67 USD / Hour

Microsoft Corporation

Expiration Date

Until further notice

Requirements

High School Diploma, GED, or equivalent
3+ years mission critical services work/applied learning experience (e.g., high availability assembly/manufacturing/critical infrastructure environments such as data centers, oil and gas refineries, hospitals, pharmaceutical, manufacturing, or related fields) or equivalent experience
1+ year(s) experience in a specialized area (e.g., mechanical field, electrical field, controls field) or related field
Ability to meet Microsoft, customer and/or government security screening requirements are required for this role
This position will be required to pass the Microsoft Cloud background check upon hire/transfer and every two years thereafter

Job Responsibility

Understands, follows, and ensures safety and security requirements (e.g., job hazard assessments [JHAs], toolbox talks), and business processes and procedures are met, to properly perform work in a safe, quality, and reliable manner in accordance to applicable Authority Having Jurisdiction (AHJ) regulations, and Microsoft requirements
Processes method statement of work (MSOW) documents
Coordinates activities and associated schedules with contractors
Performs inspections of equipment in a facility
Participates in testing and commissioning activities
Advises engineer partners or project management colleagues on project scope process or execution methodology
Prepares and submits highly complex reports as assigned following preexisting scripts and templates, or using ad hoc methods required to support trending and analysis (e.g., Root Cause Analysis [RCA] reports) and may review prior reports delivered by less experienced team members
Develops methods of operating procedure (MOPs), standard operating procedures (SOPs), and/or digital methods of operating procedures (DMOPs) for highly complex and/or interdependent equipment and disciplines to ensure safe and reliable execution
Reviews completed work using approved tools and procedural templates from less experienced technicians for accuracy and completeness
Completes and provides coaching to support less experienced technicians for mandatory, technical, and procedural training assignments

Fulltime

Experienced pharmaceutical operator

Randstad

Location:
Canada , Mississauga

Category:
Manufacturing

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
March 10, 2026

Expiration:
April 27, 2026

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Randstad

Location:Canada , Mississauga

Category:Manufacturing

Contract Type:Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:March 10, 2026

Expiration:April 27, 2026

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Location:
Canada , Mississauga

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Contract Type:
Not provided

Job Posted:
March 10, 2026

Expiration:
April 27, 2026