Executive - Pharmaceuticals

**Roles and Responsibilities**
- To perform product lifecycle management tasks for externally supplied products and own production products like evaluation of change controls, deviations, temperature excursions, stability data, process validation documents from Product quality point of view.
- Handling of problem-solving cases for products (includes both analytical and formulation related changes which have impact on product quality).
- Overall product quality evaluation and provide input during supplier's meetings.
- Follow up with suppliers and/or other stakeholders for documents related to changes for externally supplied products. E.g., possible impurities in API and finished products risk assessment in line with updated guidelines.
- Requesting, follow-up and tracking of Product Quality Review (PQRs) related data.
- Preparation and evaluation of Product Quality Review (PQRs) for externally supplied products, related coordination and follow-up with suppliers and other stakeholders.
- Writing of Product Quality Review (PQRs) for own production products and ensure its timely approval.
- Preparation and review of other documents related to Product Quality Review (PQRs).
- Responsible for planning stability studies, writing and/or review of stability protocols, reports and preparation of technical documents in CTD format.
- Co-ordinate and follow up stability studies at CROs/CQC.
- Writing and/or reviewing of process validation, technology transfer, study batch documentation for own products.
- Write/check/review pharmaceutical documents as per regulatory requirements.
- Write documents into Orion’s IT systems.
- Preparation and maintenance of lists/documents/records and archiving at appropriate place.
- Co-ordination with other departments / partners.
- Achievements of responsibilities within the agreed timelines.
- To assist the overall working of Indian Pharmaceutical team.
- Other possible tasks appointed by Supervisors.

**Note: We do not have own laboratories in India**

**Primary Skills (essential)**
- Minimum 4 years' experience in Formulation R&D or API R&D activities in global Pharma industry
- Knowledge of organic chemistry/ Pharmaceutical medicinal chemistry/ synthetic chemistry will be an added advantage
- Ability to analyze the impact of change on Nitrosamine and/or other relevant physico-chemical risks assessment, if possible.
- Confirmed knowledge of EU requirements and ICH guidelines
- Practical development skills from the laboratory to the production scale concerning different types of formulations (tablets, capsules, liquids, etc.) will be considered as an added advantage.
- Fluency in oral and written English
- Task oriented with learning attitude and Teamwork skills
- Confirmed skills of Microsoft Office are essential

**This job offers**
- An excellent opportunity to work in an inspiring and important role in the area of Pharmaceuticals
- Great opportunity to become part of the wholly owned subsidiary of globally operating Orion Group
- Possibility to utilize your own strengths with the support of professionals
- Flexible, high spirit working environment where your skills are appreciated
- Good work-life balance
- Clear, transparent processes and responsible supervisors are our benefits to the personnel

**Education**

Bachelors/master's degree in pharmacy from a reputed College/University or

Master's degree in chemistry from a reputed College/University

At Orion, your work creates true impact and well-being for our customers, patients and society at large. Our culture of friendliness, respect, mutual appreciation and diversity creates a safe working environment where you can strive for excellence. We offer a wealth of career paths and development opportunities that support the development of innovative solutions and improving the quality of life.
- Required documents: CV/Resume
- Application deadline: 31.07.2025