Senior Consultant

hace 3 meses

Barcelona, España Pharmeng Technology Inc A tiempo completo

**PharmEng Technology** is a global ISO certified Pharmaceutical Compliance Consulting Firm with projects around the world providing quality services to the manufacturers of pharmaceutical and health care products for over 25 years.

Our 300+ global consultants have expertise in Commissioning & Qualification, Validation, Quality Systems, Engineering, Medical Devices, Modular Cleanrooms, Thermal Mapping, Training, Toxicology and Regulatory Affairs.

**PharmEng Technology** is a cGMP compliant leader with international offices in Canada, Spain, France, Germany, Austria, Switzerland, Italy, Belgium, Singapore, Malaysia, Indonesia, Taiwan, Ireland, Denmark, Brazil, and USA and maintains strategic partnerships for extended capabilities internationally.

**PharmEng Technology** is seeking full-time experienced **Consultant** for a project in Barcelona, Spain.

Job Overview
- Experience in the **Pharmaceutical Companies** is required.
- English is mandatory, Spanish is a plus.

**Responsibilities**:

- Provide general consulting services on behalf of the Company for the Company´s client.
- Develop resources requirement for timely completion of consulting activities.
- Develop documentation requirements for the validation process.
- Develop system for maintaining documentation required for consulting process.
- Communicate with the Company´s supervisors on a regular basis to ensure timely response to issues and progress milestones.
- Assist the delivery team to deliver the project within the defined schedule.
- Attend meetings as required.
- Review documentations such as but not limited to: URS, DS, FS, Commissioning & Qualification Protocols, and Reports.
- Contact potential clients for services for PE.
- Identify and qualify potential new business opportunities.
- Develop and manage relationships with potential new customers.
- Generate leads and proposals.
- Close new business deals.

**Qualifications**:

- Bachelor's degree in technical field (engineering, biology, chemistry, pharmacy).
- At least 7 years of experience in Biopharma or Pharma industry.
- Generation and overview qualification documents like URS, System Risk Assessment, DQ, IQ, OQ, PQ, SOPs.
- Firm understanding of cGMP validation requirements / guidelines and familiarity with EMEA and FDA regulatory requirements for the Pharmaceutical/biopharmaceutical industry.
- Proven capability to assess processes, equipment, and products for sources of variation, ability to analyse data and reach appropriate conclusions, and to perform and appropriately document deviations and investigations.
- Strong project and process management skills.
- Excellent oral and written communication skills.
- Ability to develop and contact potential clients.
- Experience with Microsoft Office Suite.
- Fluency in English is a must.

**Skills**:

- Good communication skills.
- Team Leader.
- Team player.
- Problem Solving Ability.
- Self-driven
- Attention to detail.
- Analytical Thinking.
- Stakeholder Management in a matrixed environment.

What we offer
- Full-Time Position.
- Competitive Salary.
- Opportunities working for a global company.
- Continuous Professional Improvement including, but not limited to, courses or seminars.

At **PharmEng Technology**, we don’t just accept difference — we celebrate it, we support it, and we thrive on it for the benefit of our employees, our clients, and our community. **PharmEng Technology** is proud to be an equal opportunity workplace.

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