Your responsibilties:
Projects’ management withing API Business Unit, in particular the development of manufacturing technologies of active substances in order to effectively implement the strategic goals of the Organization
Efficient planning and implementation of projects, based on best practices, in particular projects ordered by an external customers (CDMO)
Work closely with the entire API BU R&D Team and other departments/divisions to achieve defined project goals
Participation in building cross-functional CDMO organization, streamlining existing process and setting-up new ones
Project team management/leadership at every stage of its formation
Using effective communication tools to secure seamless project execution
Developing cooperation skills in the project team and organizational structure
Conflict management in the project
Effective change and risk management
We offer:
Stable employment in a modern and dynamically-developing pharmaceutical company operating in international markets
Contract of employment / B2B contract
Hybrid system of work
Employee relocation package
Company car / car allowance
Basic salary + bonuses
Private medical care
Subsidy for meals
Multisport card
Possibility to join group life insurance
Employee Pension Program
Points in the Motivizer cafeteria
Our requirements:
Higher education in chemistry or related fields will be an advantage;
Basic knowledge and experience in developing or conducting manufacturing processes of pharmaceutical substances under GMP conditions;
Practical and theoretical (supported by certificates) knowledge of project management theory;
Previous experience within CDMO organization is an advantage
Knowledge of the principles of: budgeting, risk calculation, negotiations;
High interpersonal skills, also in communication with external clients
Ability to translate project goals and client requirements to the project team
Minimum 5 years of experience in project management;
Knowledge of project management support tools is welcome, e.g. MS Project, Jira or similar
Very good knowledge of English (both spoken and written)
Very good ability to present project statuses using Ms Office or other packages
Skills Required
- Higher education in chemistry or a related field
- Basic knowledge and experience developing or conducting pharmaceutical substance manufacturing processes under GMP conditions
- Practical and theoretical knowledge of project management theory, supported by certificates
- Previous experience within a CDMO organization
- Knowledge of budgeting, risk calculation, and negotiations
- Strong interpersonal and communication skills, including communication with external clients
- Ability to translate project goals and client requirements for the project team
- Minimum five years of project management experience
- Knowledge of project management support tools such as MS Project or Jira
- Very good spoken and written English
- Strong ability to present project statuses using Microsoft Office or similar software
What We Do
Polpharma is a Polish pharmaceutical group and the country’s largest pharmaceutical manufacturer. It develops, manufactures, and supplies prescription, over-the-counter, hospital, and other medicinal products, along with active pharmaceutical ingredients, dietary supplements, and medical devices. The company operates production plants and research and development centers, exports medicines and APIs internationally, and focuses on providing safe, effective, accessible treatments across multiple therapeutic areas.
