At a Glance
- Tasks: Manage new equipment delivery and improve manufacturing processes in the pharmaceutical industry.
- Company: Leading pharmaceutical company focused on innovation and safety.
- Benefits: Competitive salary, full-time hours, and opportunities for professional growth.
- Other info: Diverse workplace promoting equality and excellent career advancement opportunities.
- Why this job: Join a dynamic team making a real difference in drug manufacturing.
- Qualifications: Degree in Chemical or Pharmaceutical Engineering and 5 years of relevant experience.
The predicted salary is between 51750 - 63250 £ per year.
- Process Engineer - Pharnmaceutical
- Salary
- Competitive Salary
- Location
- Sandwhich, Kent – Office Based Contracted Hours Permanent – Full Time
- Job Overview
The Process Engineer is a role in the manufacturing team in Sandwich.
This position manages the delivery of new equipment/technology via continuous improvement as part of the site capital projects program.
It provides process safety support to ensure the facilities manufacturing processes are capable of meeting the processing demands of the latest generation of Drug Substance Targets and their intermediates.
Duties & Responsibilities
- Provides process engineering support to the PDF to ensure it meets operational requirements and all applicable legislative and corporate standards.
Complies with all aspects of current Good Manufacturing Practices.
- Supports the ongoing capital development of operations and process facilities by defining and clearly specifying requirements, and then collaborating with external vendors, facilities, and engineering groups to deliver and implement the appropriate design solution.
- Project manage and provide technical expertise to capital projects from initial conceptual design, through detailed design, installation, and commissioning/validation.
Ensure that projects are completed on schedule and to budget following all applicable corporate and regulatory guidance/requirements.
- Leads the definition of validation requirements and standards including writing, review and technical assessment of validation protocols, commissioning and start up.
- Leads specialist safety reviews and Process Hazard Assessments (PHA) including What-If evaluations, HAZOP, LOPA, and Failure Mode & Effects Assessments, when required.
- Provides process safety engineering support to the PDF to meet Operational requirements & applicable Legislative and Corporate standards.
- Reviews changes for technical accuracy and applicability to ensure the proposed change meets operational requirements while adhering to Good Engineering Practice and EHS/Quality requirements as required.
- Provide expertise to the Pilot Plant or Laboratories by bringing knowledge of chemical engineering concepts and techniques to solve practical development and plant operational problems.
- Leads or participates in Quality and Safety investigations.
- All other duties as assigned.
- Essential Experience Requirements - Knowledge, Skills, & Abilities (KSAs)
- Degree in Chemical Engineering, Pharmaceutical Engineering, or related engineering discipline. (BEng, MEng, BSc)
- Minimum of 5 Years relevant experience within a manufacturing environment.
- Competent in equipment specification, purchase, and related tasks.
- Experience in HAZOP, LOPA, and process safety analysis.
- Capable of writing and reviewing commissioning or validation protocols and technical documents.
- Strong communication, teamwork, and adaptability skills.
Desirable Experience Requirements
- Experience in the delivery of capital projects within a pharmaceutical environment or similar industry such as Chemical or FMCG.
- Knowledge of chemical engineering principles applied to drug substance manufacturing.
- Experienced in leading Process Safety technical discussions.
- An understanding of engineering controls required to manage high potency compounds.
Westin Par values diversity and promotes equality.
No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010.
Candidates must be eligible to live and work in the UK.
For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies, we are acting as an Employment Agency.
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Process Engineer - Pharmaceutical employer: Artemis Clarke Ltd
Artemis Clarke Ltd is an exceptional employer, offering a vibrant work culture at Bluewater that fosters teamwork and personal growth. With a focus on employee development through training opportunities and a competitive bonus scheme, we ensure our Store Managers are well-equipped to lead their teams to success while enjoying attractive employee discounts. Join us to be part of a dynamic retail environment where your passion for sales and leadership can truly shine.
StudySmarter Expert Advice🤫
We think this is how you could land Process Engineer - Pharmaceutical
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✨Tailor Your Approach
When you're applying for roles, don't rush it! Take the time to customise your applications for specific positions, showcasing relevant skills and experiences that align with what Artemis Clarke Ltd is looking for. A tailored application can really make you stand out!
We think you need these skills to ace Process Engineer - Pharmaceutical
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Artemis Clarke Ltd!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show Artemis Clarke Ltd that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at Artemis Clarke Ltd!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At Artemis Clarke Ltd, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at Artemis Clarke Ltd
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Artemis Clarke Ltd that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
Take some time to familiarise yourself with Artemis Clarke Ltd’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
✨Be Ready for Regulatory Scenarios
In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.