Pharmaceutical production chemist Job at Network Scientific Recruitment (Preston)

Analytical Chemist

SRG is working with a pharmaceutical company in Loughborough. We are looking for...

Location

United Kingdom , Loughborough

Salary:

15.31 GBP / Hour

SRG

Expiration Date

Until further notice

Requirements

Bachelor's degree in a Chemistry, Pharmaceutical, or analytical related degree
Strong understanding of HPLC, GC, MS, UPLC and UV, working to GMP standards
Highly desirable: Experience testing pMDIs or inhaled products
Excellent attention to detail and organisational skills
Ability to work independently and as part of a team.

Job Responsibility

Conduct and document analytical testing (HPLC) of pMDIs, following cGMP requirements, delivering to plan on time in full
Ensure quality of data delivered is fit for purpose, whilst working in a fast, flexible environment, with a strong focus on right first time
Represent the department in a professional manner as and when required, when interacting with both internal and external customers and regulators
Establish continuous improvement as part of normal everyday work.

Fulltime

Process Development Senior Scientist

Join Amgen's Mission of Serving Patients. At Amgen, if you feel like you're part...

Location

United States , Cambridge

Salary:

123777.00 - 167463.00 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree PhD OR PharmD OR MD and relevant post-doc where applicable completed by August 2026
OR Master's degree and 3 years of Scientific experience
OR Bachelor's degree and 5 years of Scientific experience

Job Responsibility

Design and develop synthetic routes and scalable chemical processes for the manufacture of synthetic and hybrid drug substances
Develop safe, robust, efficient, and cost-effective manufacturing processes suitable for clinical and commercial production
Advance enabling technologies that accelerate pharmaceutical development and improve sustainability, efficiency, and process robustness
Support cGMP manufacturing activities and assist with technology transfer efforts to internal manufacturing sites and external contract manufacturing organizations (CMOs)
Build process understanding through experimentation, process characterization, modeling, and data analysis to ensure consistent process performance
Contribute to cross-functional drug substance development teams by providing technical expertise, experimental data, scientific recommendations, and clear documentation
Collaborate across disciplines to support regulatory filings and author technical sections of regulatory documentation
Stay current with advances in synthetic organic chemistry, process chemistry, and related technologies, and apply new scientific insights to ongoing programs
Effectively collaborate within multidisciplinary teams that include chemists, engineers, analytical scientists, and other technical experts
Independently manage project activities and deliver high-quality results within established timelines

What we offer

Health and welfare plans for staff and eligible dependents
Financial plans with opportunities to save towards retirement or other goals
Work/life balance
Career development opportunities
Retirement and Savings Plan with generous company contributions
Group medical, dental and vision coverage
Life and disability insurance
Flexible spending accounts
Discretionary annual bonus program
Stock-based long-term incentives

Fulltime

Intern (Quality)

The role supports the Quality Control (QC) / Quality function by observing and a...

Location

Pakistan , Karachi

Salary:

Not provided

GSK

Expiration Date

Until further notice

Requirements

Pharmacist / Chemist / Microbiologist / Science undergraduate
Basic understanding of pharmaceutical sciences, chemistry, microbiology, or related scientific disciplines
Interest in quality control, laboratory testing, and GMP implementation
Willingness to learn analytical techniques (HPLC, spectrophotometry, microbiological methods)
Awareness of safe and organized storage of pharmaceutical products and operations
Attention to detail, strong documentation discipline, and focus on product quality and safety
Ability to work collaboratively with cross-functional teams and support departmental projects

Job Responsibility

Observe routine testing of raw materials, intermediates, and finished products to verify compliance with defined quality specifications
Learn and support activities related to identifying impurities and contaminants to maintain product integrity
Develop understanding of applicable regulatory requirements, guidelines, and GMP and support their implementation in daily work
Contribute to the continuous improvement of product quality and safety
Observe microbiological testing to ensure product sterility where applicable
Build understanding of quality control principles, methodologies, and documentation practices
Learn to analyze samples using techniques such as HPLC, spectrophotometry, and other relevant analytical methods
Support and focus on stability studies to assess and monitor product shelf life
Contribute to the implementation of departmental objectives and quality projects
Collaborate with cross-functional teams (e.g., Production, QA, Microbiology, Engineering) for troubleshooting and problem-solving

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

Regulatory Affairs Specialist

Regulatory Affairs - office based - Bogota. ICON plc is a world-leading healthca...

Location

Colombia , Bogota

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

Bachelor's degree in Pharmaceutical Chemist or next to graduate required
Minimum 1 year of experience in regulatory area within the pharmaceutical or biotechnology industry
Knowledge or awareness of current regional guidelines and regulations is preferred
Technical knowledge in the preparation of a dossier is desirable
Prior experience using computerized information systems required: PC Windows, word processing and electronic spreadsheets
Advanced English level

Job Responsibility

Manage activities associated with obtaining initial, amendment and other central authority approvals i.e. Regulatory Agency (RA), and any other central authorities for the assigned country/ countries
Perform submission and maintenance of new health records, renovations and modifications to keep the products on the market according to the strategic plan established by the company, current Colombian laws and current local health legislation in accordance with the corporate guidelines and policies, procedures and premises
Review of promotional materials for products for human use of their therapeutic line(s) in Veeva Vault or current tool
Perform submission and monitoring of products for human use of their therapeutic line(s) in procedures such as: PSUR, DSUR, RMPs, and safety information according to current Colombian regulations
Back-up to the Head of Regulatory Affairs and analysts of records in the procedures of INVIMA in order to guarantee the operation of the area
Ensure that IP labels are in adherence to country requirements and submitted where applicable
Support the senior level regulatory staff/country consultant in the maintenance of accurate, up-to date Country Knowledge repositor
Contribute to the maintenance and collection of regulatory intelligence by ensuring that tools such as the Country Knowledge Repository and the Country Fact Sheets are up-to-date and communicate new information or changes to the Regulatory Intelligence Consultant team
Preparation of electronic regulatory submission of post-registration requests, HMPs, Labeling notifications, additions, publication corrections and database corrections, among other petitions to be field at MoH
Follow-up on the status of the regulatory submissions (paper dossiers) from dispatch to the receipt of proof of protocol

What we offer

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others

Fulltime

Chemist - Afternoon shift (Saturday to Wednesday 15:00-23:30)

At Baxter, we believe every person—regardless of who they are or where they are ...

Location

Canada , Alliston

Salary:

72080.00 - 108120.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

University Degree or equivalent experience, Bachelor of Science Majoring in Analytical Chemistry or Biochemistry
3-5 years of analytical chemical testing lab experience
Over 2 years of chemical lab experience in a pharmaceutical industry is preferred
Familiarity with laboratory equipment in a Quality Management Laboratory
Proficiency in MS Office and laboratory computerized systems
Must have strong organizational and time management skills
Highly effective analytical and problem-solving skills and critical thinking abilities
Highly effective communication and interpersonal skills
Experience performing analytical testing in compliance with specification requirements, including instrumental techniques such as HPLC, ICP-MS, GC, Atomic Absorption, UV-VIS spectroscopy, Flame Photometry, and IR spectroscopy
Knowledge of GMP, ISO, and regulatory requirements

Job Responsibility

Perform chemical analysis to ensure product acceptability
Ensure that final products meet required standards before release by analyzing them using instrumental and wet chemical techniques according to the specifications
Analyze in-process samples using a variety of assays and procedures, taking appropriate action if the result is out of the specified limits
Maintain chemistry lab in good order
Compile analysis reports by entering results into the Laboratory Information Management System (LIMS), approving them, and forwarding to the Document Center
Support departmental 6S efforts by maintaining all work areas in a clean and orderly state, disposing of waste, cleaning glassware, and removing expired chemicals/reagents
Perform required preventative maintenance on equipment in the QM lab to ensure accurate functioning and delivery of consistent and reliable results
Contact manufacturers of equipment and arrange for service in the event of equipment malfunction

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer
Employee Stock Purchasing Plan
Defined contribution pension plan
medical/dental benefits on your first day

Fulltime

Medical Representative

We are hiring Medical Representatives to promote pharmaceutical products and gen...

Location

India , Nagpur

Salary:

Not provided

Randstad

Expiration Date

July 05, 2026

Requirements

Graduate in Science / Pharmacy or related field
Good communication and interpersonal skills
Knowledge of Nagpur territory preferred
Willing to travel locally

Job Responsibility

Doctor and chemist visits for product promotion
Achieve monthly sales targets
Build and maintain strong customer relationships
Conduct product detailing and promotional activities
Market feedback and competitor analysis

What we offer

Industry-best salary + incentives
TA/DA and other benefits
Training and growth opportunities

Fulltime

Territory Executive - Medical Representative

We are seeking a proactive and professional Territory Executive to join our team...

Location

India , Patna

Salary:

Not provided

Randstad

Expiration Date

July 09, 2026

Requirements

Any Graduate degree is acceptable
Maximum of 5 years of experience in a similar role
Proficiency in Doctor meetings, and chemist and stockist meetings
Strong understanding of the Pharma/Healthcare/Lifesciences industry
Excellent communication and interpersonal skills
Ability to work independently and manage a territory effectively

Job Responsibility

Engage in doctor meetings to present and promote our pharmaceutical products
Cultivate and maintain strong relationships with chemists and stockists to ensure product availability and drive sales
Develop and execute territory-specific strategies to achieve sales targets and market penetration
Gather market intelligence and provide feedback on competitor activities and market trends
Manage territory operations efficiently to maximize coverage and impact

Medical Representative

We are hiring Medical Representatives to promote pharmaceutical products and gen...

Location

India , Bishrampur

Salary:

Not provided

Randstad

Expiration Date

July 05, 2026

Requirements

Graduate in Science / Pharmacy or related field
Good communication and interpersonal skills
Knowledge of Bishrampur territory preferred
Willing to travel locally

Job Responsibility

Doctor and chemist visits for product promotion
Achieve monthly sales targets
Build and maintain strong customer relationships
Conduct product detailing and promotional activities
Market feedback and competitor analysis

What we offer

Industry-best salary + incentives
TA/DA and other benefits
Training and growth opportunities

Fulltime

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Pharmaceutical production chemist

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