Chemistry Analyst (Quality Control)
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We Are Teva
We’re Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it’s innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we’re dedicated to addressing patients’ needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together.
A Day In The Life Of A Chemistry Analyst
As a Chemistry Analyst you will carry out Material and Product analysis in order to supply quality products to customers and meet department objectives.
Key Responsibilities
Test and analyse components/raw materials/bulk/CIP samples/water systems and finished product using the correct procedures in compliance with cGLP, cGMP, Health and safety, SOPs and environmental and regulatory requirements.
Deliver high customer service to all customers by testing components/raw materials/bulk and finished product in an efficient and timely manner.
Process, maintain and archive all QC documentation, right first time, i.e. correct and in full, in order to achieve customer service and GMP.
Establish performance/development goals. Maintain training records accurately, ensuring compliance with regulatory and business standards.
Monitor and purchase laboratory consumables ensuring availability for timely testing of all samples.
Ensure performance of instrument maintenance and calibration checks.
Assist with the method transfer process ensuring timely completion in line with manufacturing plans.
Assist with qualification studies on existing and new methods.
Your Skills and Experience
Do you have?
Science degree in a relevant discipline and/or position specific experience
Working lab experience ideally before but should have experience through education
Pharmaceutical experience operating to regulatory standards is desirable
Understanding of cGMP/GLP/Regulatory/Health and safety - desirable
Good knowledge of Laboratory instrumentation (such as FT-IR, UV-Vis, HPLC) desirable but not required: SoloVPE. PA800 and SmartScope
Are you?
A good communicator and team worker with the ability to deliver high performance standards relating to Quality, Safety, cost and customer service
Someone who has excellent attention to detail
Able to follow procedures and processes closely
How We’ll Take Care of You
At Teva, better health starts from within, and that includes you. From day one, you’ll be supported with benefits designed to help you thrive in and out of work. This includes generous annual leave, reward plans, flexible working schedules (dependent on role), access to tailored health support, and meaningful ways to give back to the community. When it comes to your career, you’ll be encouraged to explore, evolve, and shape your path. Twist, our one-stop shop for career development platform, gives you access to a wide range of possibilities, from learning programs and short-term projects to opportunities for internal growth. Here, you’ll be part of a culture that empowers you to reach your goals and prioritize your wellbeing every step of the way.
Already Working @Teva?
Make sure to apply through our internal career site on Twist, your one-stop shop for career development
The deadline for internal applications will be Wednesday 14th October 2025
Teva’s Equal Employment Opportunity Commitment
Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.
Job details
How this role compares
Computed from every other active Quality role in our database, not just this employer's listings.
We currently track 1008 comparable Quality roles across 131 biopharma companies.
Salary context
193 of 1008 peers report a salary range (USD, annualized)
Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.
Where these roles are based
Top locations among the 1008 comparable roles
+ 42 more countries
Seniority mix
498 of 1008 peers have a known seniority level
Therapeutic area mix
2 of 1008 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
Similar opportunities
The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.
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How we calculate "similar"
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Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.