Kenvue 目前正在招聘 a：
我们做什么
在 Kenvue，我们意识到日常护理的非凡力量。我们以一个多世纪的传统为基础，植根于科学，是标志性品牌的品牌 - 包括您已经熟悉和喜爱的 NEUTRGENA®、AVEENO、TYLENOL®®、LISTERINE®、JOHNSON'S® 和 BAND-AID®。科学是我们的热情所在;关心就是我们的才能。
我们是谁
我们的全球团队由 ~ 22,000 名才华横溢的员工组成，他们的职场文化中，每个声音都很重要，每一个贡献都受到赞赏。 我们热衷于洞察， 创新并致力于为我们的客户提供最好的产品。凭借专业知识和同理心，成为 Kenvuer 意味着每天有能力影响数百万人。我们以人为本，热切关怀，以科学赢得信任，以勇气解决——有绝佳的机会等着您！加入我们，塑造我们和您的未来。有关更多信息，请单击 here.
Role reports to：
Production Lead位置：
Europe/Middle East/Africa, South Africa, Gauteng, Johannesburg工作地点：
完全现场你会做什么
Kenvue is currently recruiting for:
Production Pharmacist Interns (x2)
This position reports into the Production Lead and is based in Cape Town, South Africa.
What we do
At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent.
Who we are
Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours. For more information, click here.
Role reports to: Production Lead
Location: Cape Town, South Africa
What You Will Do
All activities executed by the Pharmacist Intern must be conducted under direct supervision of a pharmacist or tutor registered with the South African Pharmacy Council (SAPC).
Support production (dispensary, manufacturing, packaging and distribution) processes to ensure these that these processes are compliant, reliable and efficient.
Four different pillars to achieve the above goal:
- Day-to-Day Support: The Production Intern (PI) is responsible to properly support the production area to ensure in-compliance support where needed (e.g. line opening, line closing).
- Process Knowledge: The PI has to understand the production processes for which he/she is responsible. This scopes scientific understanding of the process, knowhow on production equipment within the process and identifying risks to ensure execution in compliance.
- Product Stewardship: This pillar scopes basically the ownership of the product as well as the GMP documentation in the area of responsibility. The PI will monitor the processes to ensure they are capable and in control, will participate in any changes (change controls, transfers, etc) and will facilitate root cause investigation in case deviations happen.
- Continuous Improvement: The PI should identify actions to improve the production processes and achieve leaner and more efficient practices. For this, the PI will identify improvement areas, evaluate risks and execute following Good Documentation Practices e.g. Change Control.
Key Responsibilities
Based on the four pillars
Day-to-Day Support:
- Ensure that procedures and process within area of responsibility are performed in accordance with relevant Standard Operating Procedures, Work Instructions and current Good Manufacturing Practices.
- Drive and support close out of all relevant compliance related audit findings.
- Responsible for performing line-openings and in process checks according to legislative and company requirements.
- Update GMP documents (SOP, WI, PPI and PI etc), as required and train accordingly.
- Ensure effective communication to all relevant parties.
- Ensure all production documentation and processes are completed as per cGMP guidelines.
Process Knowledge
- Understand process flow
- Understand process controls as well as risks
- Understand technically the product and its composition
- Understand process/product cost structure
- Support training to operators
Product Stewardship
- Ensure GMP, EHS and Quality compliance during the execution of the Plan and all related tasks. Ensures compliance with work instructions according to the relevant SOP's
- Perform in process audits – both planned and ad hoc accordingly to ensure that GMP standards are met and maintained.
- Support regulatory with technical documents
Continuous Improvement:
- Drive, contribute and support continuous improvement initiatives of GMP compliance and standards within the department accordingly and together with the management team.
- Plan the implementation of improvement projects
- Perform internal assessments in production areas and develop corrective actions to strengthen cGMP.
What We Are Looking For
Required Qualifications
- Registered with SAPC as a Pharmacist Intern
- B. Pharm degree successfully completed
- Good planning and administrative competencies
- Good verbal and written communication
- Logical approach to problem solving and trouble shooting
- High work standards and business ethics
- Must be available to work shifts if required
- Interpersonal skills - Active listening, provides constructive feedback, team player, communication skills
- Must be inquisitive in nature
- Deadline and target driven approach and behavior
- User knowledge of Microsoft Office
What’s In It For You
- Competitive Benefit Package
- Paid Company Holidays, Paid Vacation, Volunteer Time, Summer Fridays & More!
- Learning & Development Opportunities
- Employee Resource Groups
Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
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