Job Description and Responsibilities Reviewing packaging activity at CMO site Handling of Computerized Training Management system related activities Handling of Change Request Forms through Computerized software Preparation and Review of Certificate of Analysis (CoA) Analytical Result entries to SAP batch data Maintenance of SOPs and Internal guidelines in SAP Handling of GMP/ MIA certificate availability activity Managing various Quality Assurance documents and notifications Preparation of Report for QA activities Primary Skills (essential) 4 - 5 years’ experience in Quality Assurance (preferably Pharmaceuticals)/ IPQA (Packaging) Experience in managing various Quality Assurance documents and notifications Proficient in MS Office Experience of working in ERP / SAP and computerized systems like Track wise/ DMS would be an added advantage Good English communication skills (both verbal & written) Good Interpersonal Skills Ability to work in team and flexibility to adapt to change Education Bachelors/ Master's degree in Pharmacy / Science from a reputed College / University
Roles and Responsibilities Coordinate and follow-up with internal and external partner to review and evaluate Nitrosamine impurity and ensuring compliance to relevant guidelines. Managing and developing the process for Excipient GMP risk evaluation including maintenance of the structure with functionalities. Review elemental impurities statement, its impact on final product and ensuring compliance. 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 contract research organizations (CROs)/ Chemical Quality Control lab of Orion (CQC). Co-ordinate and follow up validation and method transfer at CROs. Write/check/review analytical and pharmaceutical documents as per regulatory requirements (method and validation documents/ variations/ additional question responses) Evaluate/ review method validation protocols / reports / analytical methods prepared by CROs. Reviewing and commenting on change controls, deviations, temperature excursions, stability data, process validation documents and troubleshooting etc. for externally supplied products. Write documents into Orion’s IT systems for example analytical methods Writing of Product Quality Review (PQRs) for own production products and ensure its timely approval. Preparation and review of other documents related to PQRs. Requesting, follow-up and tracking of PQR related data. Review of Externally supplied PQRs, related coordination and follow up with vendor and and other stakeholders Theoretical evaluation of physico-chemical properties of the drug products and/or raw materials Co-operation with other departments/ partners Local in-licensing support 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' work experience in Analytical Development or Pharmaceutical product development or Quality Assurance activities in global Pharma industry Knowledge of EU and US requirements and ICH guidelines Practical development skills from the laboratory work and troubleshooting Task oriented with learning attitude and Teamwork skills Fluency in oral and written English Confirmed skills of Microsoft Office is essential Pharmaceutical education & practical analytical development skills also from the laboratory to production scale of different types of formulations (tablets, capsules, liquids, etc.) will have added advantage Candidate interested/experienced in above documentation work will be preferred. 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 the 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 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. Please visit our website to find further information about our values and Orion as an employer https://www.orion.fi/en/careers/orion-as-an-employer/ . How to apply and additional information Please fill Candidate Information Form on https://forms.gle/o9BhfmhigBcyp5fy7 & email your CV to [email protected] Required documents: CV/Resume Application deadline: 05.07.2025
Description of position You will work as a technical expert in Laboratory IT service as well as provide application support related to the laboratory systems. You will work in close cooperation with business administrators, colleagues from the Orion Information Management team and infra service providers for technical implementations, troubleshooting and technical changes. Key responsibilities: Managing system configuration, enhancement and life cycle Providing 2nd level application support and utilizing 3rd level support Problem solving of various technical issues related to different phases of systems life cycle Appropriate technical and user testing and documentation to comply with the industry regulations Acting as a subject matter expert in concepting, implementation and upgrade projects Understanding Laboratory systems and processes to match the demand with an optimal solution and/or configuration Description of unit The Business Solutions OT team is a team of Service Managers, Solution Experts, System Specialists and Solution Architect specialized to support and develop the IT systems in laboratories and production. We offer Orion's Information Management supports Orion’s success with data, digital services and solutions. As a member of this community, you are able to contribute and effect on how Orion improves well-being of our customers. We have a good working atmosphere based on common values and mutual trust. Read more about Orion as an employer. Requirements Required skills and competences needed for this role: Experience on application support and lifecycle management in a corporate organization IT technical knowledge on e.g. database, servers, network, AD, SSO, DNS, firewalls, API keys Ability to understand business needs and translate those into small enhancements or solutions Capability to manage architectural concepts of own solutions Ownership, initiative and drive. You can take accountability of the issues that occur and are motivated by solving problems and seeing the results of your work in effective use Excellent collaboration and communication skills, positive “can do” attitude as well as taking responsibility Team and business first mindset, ability to work, collaborate and communicate effectively with various cross-functional stakeholders Fluent language skills in Finnish and English Considered as an advantage: Experience in Laboratory systems, like e.g. LIMS, CDS, ELN, LES Experience of managing applications in regulated life sciences / pharmaceutical industry Service Management Framework knowledge Experience in multivendor environment
Roles and Responsibilities 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 contract research organizations (CROs)/ Chemical Quality Control lab of Orion (CQC). Co-ordinate and follow up validation and method transfer at CROs. Write/check/review analytical and pharmaceutical documents as per regulatory requirements (method and validation documents/ variations/ additional question responses) Evaluate/ review method validation protocols / reports / analytical methods prepared by CROs. Reviewing and commenting on change controls, deviations, temperature excursions, stability data, process validation documents and troubleshooting etc. for externally supplied products. Write documents into Orion’s IT systems for example analytical methods Writing of Product Quality Review (PQRs) for own production products and ensure its timely approval. Preparation and review of other documents related to PQRs. Requesting, follow-up and tracking of PQR related data. Review of Externally supplied PQRs, related coordination and follow up with vendor and and other stakeholders Theoretical evaluation of physico-chemical properties of the drug products and/or raw materials Co-operation with other departments/ partners Local in-licensing support 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' work experience in Analytical Development or Pharmaceutical product development or Quality Assurance activities in global Pharma industry Knowledge of EU and US requirements and ICH guidelines Practical development skills from the laboratory work and troubleshooting Task oriented with learning attitude and Teamwork skills Fluency in oral and written English Confirmed skills of Microsoft Office is essential Pharmaceutical education & practical analytical development skills also from the laboratory to production scale of different types of formulations (tablets, capsules, liquids, etc.) will have added advantage Candidate interested/experienced in above documentation work will be preferred. 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 the 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 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. Please visit our website to find further information about our values and Orion as an employer https://www.orion.fi/en/careers/orion-as-an-employer/ . How to apply and additional information Please fill Candidate Information Form on https://forms.gle/o9BhfmhigBcyp5fy7 & email your CV to [email protected] Required documents: CV/Resume Application deadline: 18.07.2025
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. Candidate having knowledge of theoretical and/or possible Physico-chemical risks for products based on appropriate available data (E.g., evaluation of synthesis route of API, excipients, packaging materials details etc.) will be an added advantage. 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 Candidate having interest and/or experience in pharmaceuticals documentation or any relevant pharmaceutical formulation / manufacturing related documentation will be preferred. 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. Please visit our website to find further information about our values and Orion as an employer https://www.orion.fi/en/careers/orion-as-an-employer/ . How to apply and additional information Please fill Candidate Information Form on https://forms.gle/o9BhfmhigBcyp5fy7 & email your CV to [email protected] Required documents: CV/Resume Application deadline: 31.07.2025
You will work as a technical expert in Laboratory IT service and provide application support related to laboratory systems. Your role involves collaborating closely with business administrators, colleagues from the Orion Information Management team, and infra service providers for technical implementations, troubleshooting, and technical changes. Your key responsibilities include managing system configuration, enhancement, and life cycle, providing 2nd level application support, and utilizing 3rd level support. You will be responsible for problem-solving various technical issues related to different phases of systems life cycle. Additionally, you will conduct appropriate technical and user testing and documentation to comply with industry regulations. As a subject matter expert, you will be involved in concepting, implementation, and upgrade projects, ensuring optimal solutions and configurations that match the demands of Laboratory systems and processes. The Business Solutions OT team, where this role is situated, consists of Service Managers, Solution Experts, System Specialists, and Solution Architects specialized in supporting and developing IT systems in laboratories and production. Orion's Information Management community supports Orion's success with data, digital services, and solutions. As a member of this community, you can contribute to Orion's efforts in improving the well-being of customers. The work environment is built on common values and mutual trust. Requirements for this role include experience in application support and lifecycle management in a corporate organization, IT technical knowledge (e.g., database, servers, network, AD, SSO, DNS, firewalls, API keys), the ability to understand business needs and translate them into enhancements or solutions, capability to manage architectural concepts of own solutions, ownership, initiative, and drive to solve problems and see results, excellent collaboration and communication skills, positive attitude, and responsibility. A team and business-first mindset, along with effective collaboration and communication with various stakeholders, are also essential. Fluent language skills in Finnish and English are required. Experience in Laboratory systems (e.g., LIMS, CDS, ELN, LES), managing applications in regulated life sciences/pharmaceutical industry, Service Management Framework knowledge, and experience in a multivendor environment are considered advantageous.,
Roles & Responsibilities Executive - Logistics will take the lead in managing the order and delivery process within export logistics. Responsibilities include overseeing the entire export delivery process, efficiently handling order processing, coordinating transportation logistics for export consignments, and maintaining effective communication and customer relations related to orders and deliveries. Collaboration is key, and will be working closely with internal departments (sales, warehouse) and external partners (freight forwarding agencies) to ensure the seamless operation of our logistics activities The responsibilities of the role are: Manage the entire export delivery process. Handle order processing with efficiency and accuracy. Organize transportation logistics for export consignments. Maintain effective communication and customer relations related to orders and deliveries. Collaborate closely with internal departments (sales, warehouse) and external partners (freight forwarding agencies) to ensure smooth operations Primary Skills Minimum 3 - 5 years experience in managing the order and delivery process within export logistics. Experience of working in SAP / ERP is a must Knowledge of EU requirements and ICH guidelines is desired Proven experience in export trade coordination or related roles. Excellent organizational and multitasking abilities. Proficiency in communication and negotiation skills. Ability to work collaboratively with internal and external stakeholders. Excellent English communication skills (both verbal & written) and Good Interpersonal Skills. Task oriented with learning attitude Proficient in Microsoft Office Education - Bachelors / Masters degree from a reputed College / University How to apply and additional information Email your CV on [email protected] & please share below details, Required documents, CV/Resume Current CTC, Expected CTC & Notice Period. - Application deadline - 12.09.2025 Same Posting Description for Internal and External Candidates
We are seeking a skilled SAP S/4HANA Basis Expert to manage and optimize our SAP infrastructure. This role involves overseeing the installation, configuration, maintenance, and performance of SAP S/4HANA systems, ensuring high availability and seamless integration with other IT systems. You will be part of our SAP CoE (Center of Excellence) team and be guided by the SAP Platfom lead and technical architect. SAP CoE is a midsize team responsible for SAP Platform activities, developments, and business support. We work together with an extensive partner network to enable Orion’s core business processes to be developed with the latest technologies. Key Responsibilities: System Administration: Install, configure, and maintain SAP S/4HANA systems. Perform system upgrades, patches, and support package installations. Manage database administration tasks including backup, recovery, and performance tuning. Operations & Monitoring: Monitor system performance and troubleshoot issues. Ensure high availability and disaster recovery readiness. Provide on-call support and participate in 24/7 operations as needed Integration & Collaboration: Work with cross-functional IT teams to ensure seamless integration of SAP systems. Support system migrations and landscape architecture planning. Collaborate with engineering teams to enhance cloud operations and automation. Documentation & Compliance: Maintain detailed documentation of system configurations and changes. Implement and maintain security measures to protect system data. Ensure compliance with internal and external audit requirements Primary Skills (essential) While experience is valued, we are open to hiring freshers who demonstrate strong potential Good to have understanding of SAP architecture and system components. Keen to learn and ready to take the ownership Strong problem-solving and analytical skills. Education: Bachelor's degree in Computer Science, Information Technology, or a related field. This job offers: Work with cross-functional teams.The job involves coordination with various departments, strengthening collaboration and communication abilities. Possibility to utilize your own strengths with the support of the professionals Flexible, high-spirit working environment where your skills are appreciated Good work-life balance with Hybrid way of working Clear, transparent processes and responsible supervisors are our benefits to the personnel
THIS POSITION IS FOR FRESHER GRADUATE ONLY Key Responsibilities: Design, implement, and maintain SAP roles and authorization concepts (including S/4HANA, Fiori, and other modules as applicable). Support user and role administration, including provisioning, de-provisioning, and role changes. Conduct regular audits and reviews of user access to ensure compliance with internal policies and external regulations Collaborate with internal audit, compliance, and business teams to support access control requirements. Troubleshoot authorization issues and provide support to end-users and project teams. Maintain documentation of authorization concepts, processes, and procedures. Monitor and improve SAP security performance and proactively identify risks. Primary Skills (essential) While experience is valued, we are open to hiring freshers who demonstrate strong potential Good to have understanding of SAP architecture and system components. Keen to learn and ready to take the ownership Strong problem-solving and analytical skills. Excellent communication and documentation abilities. Good to have knowledge of SAP GRC Access Control and Fiori and S/4HANA authorization concepts This job offers: Work with cross-functional teams.The job involves coordination with various departments, strengthening collaboration and communication abilities. Possibility to utilize your own strengths with the support of the professionals Flexible, high-spirit working environment where your skills are appreciated Good work-life balance with Hybrid way of working Clear, transparent processes and responsible supervisors are our benefits to the personnel Education - Bachelor's degree in Computer Science, Information Technology, or a related field