What are the responsibilities and job description for the Technical Writer position at Siegfried?
At its locations around the world, Siegfried offers employees exciting career opportunities in international settings. We cultivate multidisciplinary cooperation and encourage our staff to actively shape and influence their careers. This approach, coupled with our dynamic working environment, make Siegfried an attractive employer.
Your role
The incumbent supports the operations group and specifically the process engineering/Chem Development/Operations group in writing and maintaining production records. This includes, but is not limited to, preparing batch log records, cleaning log records, deviations, work instructions, RM specs, Intermediate specs, API specs and other documents as needed.
Works closely with Process Engineering, Quality Systems, and Operations departments.
Siegfried's work environment is dynamic and international. With a highly professional and motivated team, the company operates in a future-oriented business field. Siegfried possesses a unique culture that leverages cultural differences to create a competitive advantage. Siegfried places highest priority on providing a flexible, diverse and discrimination-free working environment in which employees can develop personally and professionally, advance innovation and deliver superior performance. We strive to provide a work environment where employees can take on challenging jobs and associated responsibilities that best serve their personal and technical development and can benefit from the success of our company. The company regulations in respect of compensation and career development opportunities apply to all Siegfried sites. Additional conditions of employment are governed by location-specific circumstances, legislation and customs.
Who we are
In the Midst of People’s Lives – Across the Globe
The Siegfried Group is one of the world’s leading Custom Development and Manufacturing Organizations (CDMOs) developing and producing active pharmaceutical ingredients (API), intermediates and finished dosage forms. As our core competence, we successfully integrate chemical and pharmaceutical capabilities into a single business model.
The Siegfried name stands for highest quality, efficiency, flexibility and safety. Present in Europe, Asia and North America, we serve a broad global customer base from major international pharmaceutical companies down to small biologic-pharmaceutical organizations. For them we develop and produce product innovations on a large scale to finished products. We integrate our offer seamlessly into the customers’ value chain. Our comprehensive services range from early-stage Research & Development services such as synthesis, scale-up, formulation development, stability studies and method development all the way through to manufacturing services, ranging from preclinical R&D material for clinical trial purposes to commercial production.
We are able to produce about 200 of the approximately 1500 registered drug substances used in medicine. Moreover, we produce 20 percent of global demand for caffeine. Consequently, nearly 1 billion individuals come into contact with Siegfried products.
What we do in Grafton
The Siegfried Acceleration Hub in Grafton specializes in early-phase development and manufacturing services, including services for projects with highly potent APIs.
Competencies
Your role
The incumbent supports the operations group and specifically the process engineering/Chem Development/Operations group in writing and maintaining production records. This includes, but is not limited to, preparing batch log records, cleaning log records, deviations, work instructions, RM specs, Intermediate specs, API specs and other documents as needed.
Works closely with Process Engineering, Quality Systems, and Operations departments.
- Organizes material and completes assignment according to set standards regarding order, clarity, style and terminology.
- Edit, standardize, or make changes to material prepared by others to improve ability of reader to more clearly understand.
- Work to create and maintain standardized templates for production records
- Adheres to personal moral, ethical, legal, and behavioral conduct that is in compliance with the Siegfried Code of Conduct.
- Implements and adheres to all applicable SHE, DEA, and cGMP regulations.
- Provide assistance with projects as needed and as assigned by the Head Chem Dev.
- Ability to translate verbal and generic technical process descriptions into detailed written instructions.
- A degree in Chemical Engineering, Chemistry, or other technical degree in addition to 1-3 years' experience in a pharmaceutical organization are required.
- Experience with tech transfers as well as in-depth knowledge of process engineering and cGMP regulations are required.
- Must have excellent verbal and written communication skills.
- Must be able to work efficiently with people of all levels and cultures.
- Must be a team player. -Must be highly organized and must be very conscientious and detail-oriented.
- Must be a self-starter and initiator.
- Must have good computer skills (word, spreadsheet, presentation). -Must be able to manage several complex projects/issues simultaneously
- Must have good interpersonal skills with an ability to negotiate.
Siegfried's work environment is dynamic and international. With a highly professional and motivated team, the company operates in a future-oriented business field. Siegfried possesses a unique culture that leverages cultural differences to create a competitive advantage. Siegfried places highest priority on providing a flexible, diverse and discrimination-free working environment in which employees can develop personally and professionally, advance innovation and deliver superior performance. We strive to provide a work environment where employees can take on challenging jobs and associated responsibilities that best serve their personal and technical development and can benefit from the success of our company. The company regulations in respect of compensation and career development opportunities apply to all Siegfried sites. Additional conditions of employment are governed by location-specific circumstances, legislation and customs.
Who we are
In the Midst of People’s Lives – Across the Globe
The Siegfried Group is one of the world’s leading Custom Development and Manufacturing Organizations (CDMOs) developing and producing active pharmaceutical ingredients (API), intermediates and finished dosage forms. As our core competence, we successfully integrate chemical and pharmaceutical capabilities into a single business model.
The Siegfried name stands for highest quality, efficiency, flexibility and safety. Present in Europe, Asia and North America, we serve a broad global customer base from major international pharmaceutical companies down to small biologic-pharmaceutical organizations. For them we develop and produce product innovations on a large scale to finished products. We integrate our offer seamlessly into the customers’ value chain. Our comprehensive services range from early-stage Research & Development services such as synthesis, scale-up, formulation development, stability studies and method development all the way through to manufacturing services, ranging from preclinical R&D material for clinical trial purposes to commercial production.
We are able to produce about 200 of the approximately 1500 registered drug substances used in medicine. Moreover, we produce 20 percent of global demand for caffeine. Consequently, nearly 1 billion individuals come into contact with Siegfried products.
What we do in Grafton
The Siegfried Acceleration Hub in Grafton specializes in early-phase development and manufacturing services, including services for projects with highly potent APIs.
Competencies
- Early-phase development and manufacturing
