Associate Principal Scientist Dissolution (all genders)

Bayer; Wuppertal; Vor Ort; EUR 70.000 - 90.000; Vollzeit

Zusammenfassung

A global pharmaceutical company in Wuppertal is looking for an Associate Principal Scientist in Dissolution. You will be responsible for developing and validating dissolution methods in a laboratory setting, ensuring compliance with regulatory standards. Candidates should have a pharmacy degree (preferably PhD) and experience in the pharmaceutical industry, especially in dissolution testing and analytics. This position offers a competitive salary and flexible working options.

Leistungen

Competitive salary

Flexible work arrangements

Company daycare centers

Professional development opportunities

Health checks

Qualifikationen

• Several years of experience in the pharmaceutical industry.
• In-depth knowledge of instrumental analytics.
• Experience in dissolution testing.

Aufgaben

• Develop and implement release methods for dissolution testing.
• Optimize and validate dissolution methods according to standards.
• Provide analytical support for pharmaceutical manufacturing processes.

Kenntnisse

HPLC

Laboratory automation

Mentoring

English proficiency

Ausbildung

PhD in natural science or pharmacy

Jobbeschreibung

At Bayer we’re visionaries, driven to solve the world’s toughest challenges and striving for a world where ,Health for all, Hunger for none’ is no longer a dream, but a real possibility. We’re doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and redefining ‘impossible’. There are so many reasons to join us. If you’re hungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there’s only one choice.

Associate Principal Scientist Dissolution (all genders)

You are part of the Capability Pool NCE Analytics and Clinical Release Wuppertal (NCEW) within the CMC&T cluster. The team conducts analytical project work for active pharmaceutical ingredients and drug products in accordance with GMP and collaborates closely with analytical project leads and other partners within CMC&T.

YOUR TASKS AND RESPONSIBILITIES

You are responsible for the development and implementation of release methods as a scientific expert in a laboratory team for dissolution testing in the field of analytical development, in line with scientific and regulatory standards (e.g., ICH, FDA, EMA, pharmacopoeias)

You lead the transfer and validationof dissolution methods

You continuously optimize your approach regarding the development and validation of dissolution methods within the applicable development standards

You support formulation development and validation of manufacturing processes

You provide analytical support for site transfers of pharmaceutical manufacturing processes

• You independently interpret regulatory and legal requirements and implement them in practice to ensure that methods comply to current standards

You represent analytical development as a Scientific Expert for Dissolution in interdisciplinary project teams

You evaluate existing dissolution models and continuously improve them to enhance their relevance and efficiency in the analytical environment

You are a supervisor of scientific projects related to dissolution testing (e.g., Bachelor’s, Master’s, or PhD theses)

You are accountable for authoring and defending the CMC dossier in IND / IMPDs, with a focus on dissolution testing

You continuously improve laboratory efficiency by independently evaluating and implementing new technologies, such as automation

WHO YOU ARE

You are a pharmacist (m / f / d) or have a comparable natural science degree, preferably with a PhD

You have several years of experience in the pharmaceutical industry in the areas of development, manufacturing, and testing of drug products, ideally in dissolution testing

You have in-depth knowledge of instrumental analytics (especially HPLC) and laboratory automation

You possess advanced GMP knowledge

You have experience mentoring colleagues and enjoy working collaboratively in a team

You work efficiently, in a structured manner, and demonstrate a high level of initiative

Excellent English skills, both written and spoken, complement your profile; knowledge of German is an advantage

WHAT WE OFFER

Our benefits package is flexible, appreciative, and tailored to your lifestyle, because : What matters to you, matters to us!

• We ensure your financial stability through a competitive compensation package, consisting of an attractive base pay and our annual bonus. In addition, managers can recognize special contributions by granting an individual performance award.
• Whether it’s hybrid work models or part-time arrangements : Whenever it is possible, you will have the flexibility to work how, when and where it is best for you.
• Your family is a top priority. We offer loving company daycare centers at multiple locations, support in finding childcare, time off for the care of elderly or dependent family members, summer camps for children, and much more.
• We support your professional growth by providing access to learning and development opportunities, training programs through the Bayer Learning Academy, development dialogues, as well as coaching and mentoring programs.
• We promote health awareness and opportunities for selfcare through various measures, such as free health checks with the company doctor
• We embrace diversity by providing an inclusive work environment in which you are welcomed, supported, and encouraged to bring your whole self to work

Be You. Be Bayer.

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