Quality Assurance Pharma Job at Amaris Consulting (Frosinone)

Quality Assurance Specialist, Medical Communications

Location

India

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Experienced Medical Writer (1-2 years)
Scientific background and degree (PharmD, MD, PhD or Masters)
Knowledge of IT and digital solutions
Strong attention to detail and accuracy
Ability to manage and prioritize multiple, detailed activities
Results-orientated with fast and focused execution
Good communication, coordination and time management skills
Ability to work within a team or across multiple teams (including remotely) as well as independently
Fluent in oral and written English with high level of communication skills
Values teamwork, collaboration, and innovation

Job Responsibility

Cross check scientific information against cited references and ensure medical accuracy (fact check)
Ensure consistency with product label where applicable
Verify presence of essential information
Correct interpretation of scientific data from reference/sources
Alignment/formatting of content as per style guides/journal guidelines/congress guidelines
Ensure consistency of scientific content across different sections (including text, figures, tables)
Accurate bibliography/in-text citation and alignment of figures/graphs as per branding guidelines
Confirm that every sentence is source annotated, and each source annotation matches with respective reference and vice versa
Ensure that information is presented in a neutral manner without any interpretations and/or author’s conclusion
Track work and communicate with client team on job reviews, prioritization etc., through emails and teleconferencing if needed

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

Supt, Quality Assurance

This is where you make a difference in our patients’ safety. As a member of the ...

Location

Mexico , Tultitlán, Ciudad de México

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Bachelor's degree in QFB or similar
NOM (Pharma y Medical Devices) validation and compliance: 059, 241, 073, 072, 240, 137
FEUM compliance
Knowledge in Quality Management Systems for drugs
Analytical transfers (Quality Control)

Job Responsibility

Carry out activities related to Quality Assurance in the Distribution and storage center for medicines and medical devices
Activities of Sanitary Responsibility or Assistant to the Sanitary Responsible
Quality Assurance activities, responsible of QA for Baxter's Distribution and Storage center located in Tultitlán
Product batch validation and release
Coordinate activities related to: QSM (Quality Management System) for warehouses
Quality management for stabilities and product release
Coordinate QA team in laboratory and warehouse
Lead and guide audits related to product quality

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Fulltime

Superintendent, Quality Assurance

This role will be responsible for carrying out activities related to Quality Ass...

Location

Mexico , Tultitlán, Ciudad de México

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Bachelor's degree in QFB or similar
NOM (Pharma y Medical Devices) validation and compliance: 059, 241, 073, 072, 240, 137
FEUM compliance
Knowledge in Quality Management Systems for drugs
Analytical transfers (Quality Control)

Job Responsibility

Carry out activities related to Quality Assurance in the Distribution and storage center for medicines and medical devices
Activities of Sanitary Responsibility or Assistant to the Sanitary Responsible
Quality Assurance activities, responsible of QA for Baxter's Distribution and Storage center located in Tultitlán
Product batch validation and release
Coordinate activities related to: QSM (Quality Management System) for warehouses
Quality management for stabilities and product release
Coordinate QA team in laboratory and warehouse
Lead and guide audits related to product quality

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Fulltime

Supt, Quality Assurance

This is where you make a difference in our patients’ safety. As a member of the ...

Location

Mexico , Tultitlán, Ciudad de México

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Bachelor's degree in QFB or similar
NOM (Pharma y Medical Devices) validation and compliance: 059, 241, 073, 072, 240, 137
FEUM compliance
Knowledge in Quality Management Systems for drugs
Analytical transfers (Quality Control)

Job Responsibility

Quality Assurance activities, responsible of QA for Baxter's Distribution and Storage center located in Tultitlán
Product batch validation and release
Coordinate activities related to: QSM (Quality Management System) for warehouses
Quality management for stabilities and product release
Coordinate QA team in laboratory and warehouse
Lead and guide audits related to product quality

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Associate director lead gcp clinical quality assurance

Responsible for execution and performance of Lantheus CQA quality system element...

Location

United States , Remote

Salary:

139000.00 - 232000.00 USD / Year

Life Molecular Imaging

Expiration Date

April 15, 2026

Requirements

Bachelor’s degree in a scientific discipline preferred
Minimum 7 years’ experience in the pharmaceutical or biotech industry with five (5) or more of those years in GCP Clinical Quality Assurance
Proficient understanding of ICH GCP and appliable CFR regulations with a working knowledge of cGLP
Experience providing GCP Clinical Quality Assurance guidance to Clinical teams for assigned Programs/Trials
Experience in risk-based quality management systems and quality by design in Phase I thru IV clinical trials
Experience in conducting internal and external GCP audits (Ie. Investigational Site Audits, Process Audits, Vendor Audits etc.), authoring audit reports, managing resulting CAPA process
Ability to manage processes with continuous improvement approach
Analytical and critical thinking skills
Diplomatically work and collaborate cross functionally at all levels within the organization
Excellent communication (Oral and Written), planning, coordination, and time management skills

Job Responsibility

Serve as the CQA lead for assigned trials and assigned compliance areas ensuring the timely communication of quality risk and compliance as related to GCP/cGLP
Development and execution of a risk-based clinical quality audit plan for assigned programs
Audit internal processes, clinical investigator sites, and vendors to assess compliance with applicable regulations/guidelines and evaluate accuracy and quality of scientific data as needed
Analyze and trend audit observations, gaps, and systematic issues to support continuous improvement within pre-clinical/clinical development programs, vendors, and cross-functional groups
Evaluate adequacy and completeness of CAPAs originated from audits, deviations, and/or inspections and perform effectiveness checks
Author audit reports and coordinate supporting documentation
manage same in QMS
Peer review reports authored by colleagues
Identify non-compliance trends and systematic risks for assigned areas of responsibility
Contribute to the development, maintenance, and continuous improvement of the quality system processes, tools, and E-Systems

What we offer

Discretionary performance-based cash incentive
Discretionary annual equity award (depending on level)
Comprehensive health benefits package (medical, prescription drug, dental, and vision coverage)
Life and disability benefits
Pre-tax accounts
401(k) with company contribution
Generous time off package (paid vacation, holidays, sick days, and paid parental leave)

Fulltime

Mq ts downstream associate

The MQ TS Downstream Associate is responsible for primary contact of quality on ...

Location

India , Vizag

Salary:

Not provided

Pfizer

Expiration Date

Until further notice

Requirements

M. Pharma / Msc with more than 1 year experience in Manufacturing Quality Assurance / Quality Assurance / Production of a pharmaceutical manufacturing facility
Experience in the pharmaceutical industry and Quality administered systems
Sound knowledge of current Good Manufacturing Practices (part of GxP)
Ability to work effectively in a team environment, both within one's own team and interdepartmental teams
Effective written and oral communication skills.

Job Responsibility

Responsible for ensuring operating state of cGMP compliance in Terminal Sterilization, Visual Inspection and Packaging operations
Maintain regulatory compliance in accordance with cGMP practices
Ensure manufacturing policies and procedures conform to Pfizer standards
Knowledge and hands on experience in reviewing eBR and assessing the impact of AMPs exceptions with technical support/inputs from Sr. Associate or Sr. Team Leader
Review of Batch reports and Equipment audit trails
Perform Acceptable Quality level sampling, Inspection in VIDT and Batch record review and release
Perform batch start-up and end activities viz. sensor challenge tests, recipe review etc
Perform random process checks for Terminal Sterilization, Visual Inspection and Packaging
Perform Daily walkthroughs and report observations to the Sr. Team Leader
Perform Equipment breakdown assessments w.r.t to Product Quality and patient safety with technical support/inputs from Sr. Associate or Sr. Team Leader

Fulltime

Quality head

Location

India , Baddi

Salary:

Not provided

Randstad

Expiration Date

April 26, 2026

Requirements

15+ years experience in Pharma Industry with WHO-GMP

Quality Assurance Pharma

Amaris Consulting

Location:
Italy , Frosinone

Category:
IT - Administration

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
April 16, 2026

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