Media Fill - Aseptic Engineer Job at Pfizer (Rocky Mount)

Aseptic Officer

In this vital role you will provide technical leadership and oversight of asepti...

Location

United States , Thousand Oaks

Salary:

114990.00 - 139433.00 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree
Master’s degree and 2 years of operations or quality experience
Bachelor’s degree and 4 years of operations or quality experience
Associate’s degree and 8 years of operations or quality experience
High school diploma / GED and 10 years of operations or quality experience
10+ years of biopharmaceutical or medical technology experience with increasing responsibility
Bachelor’s or Master’s degree in Microbiology, Life Sciences, or a related field
Demonstrated expertise in aseptic processing, isolator operations, and media fill program management
Experience supporting regulatory inspections and contamination control initiatives in a sterile manufacturing environment
In-depth understanding of cGMPs, aseptic technique, and sterility assurance principles

Job Responsibility

Lead the Aseptic Technique Program for the suite, including routine observation of critical operations, data trending, and implementation of corrective and preventive actions (CAPAs)
Provide coaching and mentoring to operations personnel to strengthen aseptic practices and contamination control awareness
Author, review, and maintain aseptic-related SOPs, reports, and training materials to ensure alignment with current regulatory expectations and site standards
Partner closely with Quality Assurance, Validation, and other site Aseptic Officers to ensure consistent execution and knowledge sharing across functions
Represent Manufacturing during internal and external inspections, demonstrating robust understanding and control of aseptic practices
Lead the Media Fills supporting the site’s one of two isolator-based filling lines
Author and implement media fill protocols, complete final reports, and perform data trending and risk analysis
Partner with Manufacturing, Quality, and Engineering to ensure execution aligns with aseptic process design, batch records, and contamination control strategy
Evaluate results, find opportunities for process or operator improvement, and ensure timely closure of associated investigations and CAPAs
Support contamination and cross contamination control initiatives and provide aseptic expertise in investigations, deviations, and change controls

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, or for field sales representatives, a sales-based incentive plan
Stock-based long-term incentives
Award-winning time-off plans
Flexible work models, including remote and hybrid work arrangements, where possible

Fulltime

New

Scientist (EMPQ)

The consultant will develop and execute Environmental Qualification, Airflow Vis...

Location

United States , Juncos

Salary:

Not provided

Cencora

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Engineering or a Scientific field
5+ years of experience in a regulated industry
Experience with Environmental monitoring performance qualification (EMPQ) execution
Preferred experience with Aseptic Process Simulation Media Fill (MF)
Strong knowledge of cGMP/FDA regulations
Strong communication skills (oral and written)
Ability to organize and manage multiple tasks in a fast-paced environment
Attention to detail
Demonstrated problem solving and analytical skills

Job Responsibility

Develop and execute Environmental Qualification, Airflow Visualization Study (AVS) and Aseptic Process Simulation (APS) deliverables for operational readiness projects
Responsible for the Activities before Environmental monitoring performance qualification (EMPQ) execution
Responsible for the EMPQ execution & post approval
Responsible for the Air Visualization Studies
Responsible for the Aseptic Process Simulation Media Fill (MF)
Participate in project meetings, as applicable
Generate Validation Plan establishing lean strategies, as required
Develop and execute EM PQ, AVS and APS protocols for applicable systems
Develop EM PQ, AVS and APS reports for applicable systems
Evaluate, coordinate, and execute the required efforts (resources, plant support, equipment, materials, etc.) to support projects deliverables

What we offer

Medical, dental, and vision care
Comprehensive suite of benefits focusing on physical, emotional, financial, and social aspects of wellness
Support for working families (backup dependent care, adoption assistance, infertility coverage, family building support)
Behavioral health solutions
Paid parental leave
Paid caregiver leave
Training programs
Professional development resources
Opportunities to participate in mentorship programs, employee resource groups, volunteer activities

Fulltime

New

Senior QA Executive 1

You will play a key role in ensuring quality and compliance in a modern manufact...

Location

Singapore , Tuas

Salary:

Not provided

GSK

Expiration Date

Until further notice

Requirements

Bachelor’s degree in science, microbiology, biotechnology, pharmacy, engineering, or a related discipline
At least 6 years of experience in quality assurance within the pharmaceutical or biologics industry
Strong knowledge of GMP and regulatory requirements relevant to manufacturing and quality
Practical experience with deviations and CAPA processes
Experience with validation, qualification and change control practices
Good written and verbal communication skills in English

Job Responsibility

Provide QA oversight - Sterility Assurance for site manufacturing processes and products manufactured by the site
Provide QA oversight – Quality control laboratory for Microbiology and Endotoxin tests
Develop, implement, and monitor sterility assurance programme on site
Lead sterility assurance activities: sterile process oversight, container closure integrity (CCI) strategies, aseptic process simulation (media fills), and bioburden or sterility-related investigations
Develop, review and approve microbiology and sterility-related SOPs, specifications, and test methods
ensure documentation is current and GxP-compliant
Provide technical direction for microbiology method development, transfer, validation, troubleshooting, root cause analysis, and corrective/preventive actions (CAPA)
Manage deviations, OOS/OOT events and non-conformances related to microbiology and sterility
lead investigations and ensure timely regulatory-compliant reporting
Establish and maintain environmental monitoring programmes

What we offer

Competitive base salary
Annual bonus based on company performance
Flexible working options available for most roles
Learning and career development
Access to healthcare & wellbeing programmes
Employee recognition programmes

Fulltime

Senior Validation Engineer

In this role you will be serving patients through internal collaboration with Am...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree OR Master’s degree with 4 to 6 years of experience in process validation or a related field OR Bachelor’s degree with 6 to 8 years of experience in process validation or a related field OR Diploma with 10 to 12 years of experience in process validation or a related field
Prior experience serving as Validation lead for NPI or tech transfer of manufacturing processes
Relevant experience in qualification of finished drug product and packaging processes
Minimum of 6 years working in a cGMP manufacturing environment with a strong understanding of regulatory requirements and expectations
Ability to have a positive impact on others
the ability to affect the behaviors of others by connecting with and inspiring them
Direct experience with qualification/validation of primary and secondary packaging processes, including device / combination products is required
Experience with validation of synthetic API manufacturing processes is also highly desired
Prior experience with, or willingness to learn, other modalities, including biologic drug substance and aseptic drug product is also desired
The candidate should be able to travel within the JAPAC region, specifically Japan

Job Responsibility

Be an integral quality member of Amgen cross-functional contract manufacturing teams that includes but is not limited to operations, analytical science, process development, supply chain, etc.
Translate Amgen requirements into the language of the CMO
Identify and assess validation/quality risks to enable risk-based decisions
Validation document author/approver
Oversight of packaging process qualification, device and combination product qualifications
Determine appropriate sample plans and acceptance criteria for primary and secondary packaging processes
Implement statistical methods to create risk based sampling plans and acceptance criteria
Oversight of synthetic API manufacturing process validation and cleaning validation
Aseptic processing system oversight (media fill, autoclave validation, EM)
Prepare materials/documents (playbooks) for topics to be presented during audits/inspections

What we offer

Reasonable accommodation for individuals with disabilities

Fulltime

New

Process Validation Engineer

Reporting to the Senior Manager process Validation, the Process Validation Engin...

Location

United States , Bedford

Salary:

Not provided

PCI Pharma Services

Expiration Date

Until further notice

Requirements

Experience in pharmaceutical or biopharmaceutical environment in operations/engineering/manufacturing/quality environments
Proficient in the development and execution of PPQs
Review commissioning, qualification and validation related system lifecycle documentation
Combination of equipment qualification, process validation, or cleaning validation is acceptable
QA pharmaceutical experience also preferred
Validation experience with the following is highly preferred: Vacuum physics, Heat and mass transfer, Formulation, Aseptic Filling and Lyophilization, Steam Sterilization, data analysis and statistics
Engagement and knowhow with regulatory inspections and knowledgeable in current industry standards and regulatory trends as they pertain to Validation of pharmaceutical or biopharmaceutical processes
Bachelor of Science degree in Chemical Engineering, Biochemistry, Biology or related scientific discipline required with a minimum of 7 – 10 years of Pharmaceutical industry experience or combination of work experience in Validation, QA, MFG, MTS, Process Development or Engineering
Highly organized professional who is accustomed to working in a result oriented-focused, dynamic CMO environment
Professional and collaborative team player must have excellent interpersonal skills

Job Responsibility

Develop and support the detailed project plans and timelines for the execution of process validation activities
Prepare validation & change control documentation, including protocols, summary reports, etc.
Author Process Performance Qualification/ verification validation plans
Author and perform the technical review of deviations and planned deviations, change controls, perform process monitoring, perform activities for lot release
Participate in client and Regulatory Audits
Work on CAPA and QS with minimal oversight to achieve timely results
Assist with determining impact of change control on qualified process and aseptic operations
Work closely with other validation department personnel and cross-functionally with MTS, Manufacturing, Engineering, QC, Quality Assurance, and project management to achieve all project deliverables
Assist management with mentoring and training of colleagues on policies and procedures including the requirements for validation
Perform all functions associated with process validation support

Fulltime

New

Drug Product Manufacturing Associate II

The Manufacturing Associate II is responsible for executing GMP production of in...

Location

United States , San Diego

Salary:

27.09 - 31.60 USD / Hour

PCI Pharma Services

Expiration Date

Until further notice

Requirements

High school diploma required
Minimum of two (2) years of relevant experience in manufacturing, laboratory, mechanical or engineering positions
Ability to work with cross functional teams
Detail oriented with strong written and verbal communication skills
Ability to work independently, within prescribed guidelines, or as a team member
Demonstrated ability to follow detailed directions in a manufacturing GMP environment
Familiarity with cGMP, manufacturing, machine operations, and data entry
Must be familiar with Microsoft Office applications
Ability to constantly perform duties while donning aseptic gowning
Ability to constantly sit and reach to use computers and other office equipment

Job Responsibility

Execute GMP production of injectable pharmaceuticals by following all applicable SOP's
Prepare equipment and materials for GMP aseptic production
Operate equipment such as glasswashers, autoclaves, depyrogenation ovens and automated filling machines
Participate in one or more areas of the aseptic manufacturing injectable pharmaceuticals using GMP's in FDA regulated facility
Assist technical personnel with troubleshooting mechanical issues that arise with manufacturing equipment
Perform various semi-routine manufacturing tasks under the guidelines of established SOP’s and cGMP regulations
Troubleshoot manufacturing processes that are semi-complex in level under cGMP guidelines and under the supervision of management
Assist in the research and implementation of new methods and technologies to enhance operations
Prepare components, media, buffers, and other solutions as needed
Accurately document data and write/review batch records under cGMP guidelines

What we offer

Eligibility for an annual performance bonus
Paid time off
Health insurance coverage (including dental and vision)
Flexible spending account
401(k) plan

Fulltime

New

CRM Marketing Manager

The CRM Marketing Manager leads the technical and operational aspects of client ...

Location

Canada

Salary:

85000.00 - 105000.00 CAD / Year

FARBER

Expiration Date

Until further notice

Requirements

Post-secondary education in Marketing, Business, Information Systems, or a related field, or equivalent professional experience
5–8+ years of experience in CRM, lifecycle marketing, or marketing automation roles with hands-on platform ownership
Strong proficiency with marketing automation and CRM platforms (e.g., Dynamics 365, Customer Insights, Salesforce Marketing Cloud, Marketo, HubSpot, Braze, or similar)
Deep understanding of data structures, segmentation logic, consent management, automation design patterns, and QA methodologies
Proven experience partnering with IT and Data teams in complex, integrated environments
Strong analytical orientation with the ability to ensure data accuracy, diagnose issues, and support measurement integrity
High attention to detail, strong documentation discipline, and a systems-oriented mindset
Ability to operate autonomously within defined strategic direction and escalation frameworks

Job Responsibility

Own end-to-end technical delivery of lifecycle and CRM automations from technical design through build, QA, launch, monitoring, and ongoing maintenance
Translate approved program requirements into scalable technical solutions, including triggers, segmentation logic, suppression rules, branching, personalization, and cadence controls
Design automation solutions that balance performance, compliance, scalability, and maintainability
Create and maintain reusable templates, standard operating procedures, QA checklists, and build documentation to support consistent, scalable execution
Own CRM platform hygiene, including naming conventions, folder structures, versioning, and documentation standards as they relate to marketing automation
Proactively monitor automation performance to ensure accuracy, deliverability, and stability
Identify, diagnose, and resolve automation and configuration issues within the CRM platform (e.g., logic errors, journey failures, data handling issues), and partner with IT Applications for underlying system defects or integration issues
document root causes and corrective actions
Ensure technical implementations support internal governance and regulatory requirements, including consent management, opt-outs, exclusions, and contact cadence rules
Own CRM and marketing automation reporting setup, including tracking plans, tagging standards, dashboards, and monitoring routines

What we offer

Flexible work arrangements
Generous vacation- wellness days and birthday off
Extended health and dental coverage, plus virtual doctor services
Employee Assistance Program and mental health resources
Company-matching retirement savings plan
Financial support for professional development
Annual company events
Exclusive access to perks and discounts

Fulltime

New

Assistant Town Engineer

The town of Westborough seeks applications from energetic, team-oriented individ...

Location

United States , Westborough

Salary:

86292.00 - 112375.00 USD / Year

Massachusetts Municipal Association

Expiration Date

Until further notice

Requirements

Bachelor’s degree in engineering
At least five years of work experience in the design of and/or construction of public works projects
Registration as a Massachusetts Professional Engineer or Massachusetts Professional Land Surveyor
Valid driver’s license

Job Responsibility

Formal review of project plans and specifications
Preparation of documents for competitive bidding
Development of engineering estimates associated with roadway improvements, water and sewer system design and maintenance, and stormwater management

What we offer

$4,000 signing bonus available to fully qualified candidates

Fulltime

Media Fill - Aseptic Engineer

Pfizer

Location:
United States , Rocky Mount

Category:
Manufacturing

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
February 20, 2026

Expiration:
February 24, 2026

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