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Temporary Technical Writer

Location
Portsmouth, NH

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Job Description:
At Lonza, we invest in great people. We encourage our employees to challenge themselves and we offer an environment that fosters creativity and success. Headquartered in Basel, Switzerland, we operate production, R&D, and business sites around the world, including Europe, North America, and Asia. 
Our vision
We strive to be the leading supplier using science and technology to improve the quality of life.
Our mission
We work with passion, using advanced technologies, to transform life science into new possibilities for our customers.
Do you want to help us as we shape the future of this great organization?
Job Description Summary
We have a great opportunity for a person who wants to expand their technical writing skills as a Temporary Technical Writer in our MSAT Group in beautiful Portsmouth.
Building upon an already keen eye for precise and timely editing skills, the Technical Writer not only accurately and concisely edits cGMP documents while maintaining a busy document schedule but also begins to broaden their responsibilities within the Technical Writing Group, taking a more independent role. Technical Writers hone their interdepartmental management skills using resources to address comments from internal and external customers as well as regulatory agencies. Stemming from a developing understanding of documentation and manufacturing processes, Technical Writers produce excellence within documents knowing that these documents not only affect the ease of operations within the building but patient safety, drug quality, and business reputation.
Key responsibilities: 
Edit documents: Review and template documents with accurate, clear, and explicit description and justifications including not only component-related documents (buffers and medias) but either documents concerning early cell development or documents concerning cell quality and purification.
Begin to develop proficiency in either upstream or downstream processes
Create new cGMP documents with assistance from within the department
Adhere to established departmental practices and protocols
Manage document comments: Answer and translate questions into the reviewed document to meet regulatory, internal, and external requirements with the aid of document
Manage global DCFs: Perform initial review for scope, attain sign-offs and justifications, set up review meetings, etc.
Maintain and review schedules/campaigns: Notify associated departments of deadlines and keep documents within their scheduled timeframe; begin building a deep understanding of how scheduling works; communicating to group and appropriate departments concerning schedules
Interested?
What we need you to have:
Degree in life sciences preferred
Several years of biotech or pharmaceutical manufacturing industry experience
Demonstrated document editing and proofreading experience
Adept at researching
Basic knowledge of cGMP and manufacturing process knowledge
Comprehend how CAPAs (corrective actions/preventative actions) and change controls must be incorporated into a document
Demonstrated proficiency in Microsoft Office Suite; particularly Word, Excel, and Project
Strong written and oral communication skills
Initiative to identify and address potential problems
Highly organized with effective time management (ensuring completion of work tasks)
Strong attention to detail.
Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.  
Lonza.  The place to Go, Stay and Grow.
Apply Now
At Lonza, we invest in great people. We encourage our employees to challenge themselves and we offer an environment that fosters creativity and success. Headquartered in Basel, Switzerland, we operate production, R&D, and business sites around the world, including Europe, North America, and Asia.
Our vision :
We strive to be the leading supplier using science and technology to improve the quality of life.
Our mission :
We work with passion, using advanced technologies, to transform life science into new possibilities for our customers.
Do you want to help us as we shape the future of this great organization?
Job Description Summary
We have a great opportunity for a person who wants to expand their technical writing skills as a Temporary Technical Writer in our MSAT Group in beautiful Portsmouth. Building upon an already keen eye for precise and timely editing skills, the Technical Writer not only accurately and concisely edits cGMP documents while maintaining a busy document schedule but also begins to broaden their responsibilities within the Technical Writing Group, taking a more independent role. Technical Writers hone their interdepartmental management skills using resources to address comments from internal and external customers as well as regulatory agencies. Stemming from a developing understanding of documentation and manufacturing processes, Technical Writers produce excellence within documents knowing that these documents not only affect the ease of operations within the building but patient safety, drug quality, and business reputation. Key responsibilities: Edit documents: Review and template documents with accurate, clear, and explicit description and justifications including not only component-related documents (buffers and medias) but either documents concerning early cell development or documents concerning cell quality and purification.
Begin to develop proficiency in either upstream or downstream processes
Create new cGMP documents with assistance from within the department
Adhere to established departmental practices and protocols
Manage document comments: Answer and translate questions into the reviewed document to meet regulatory, internal, and external requirements with the aid of document
Manage global DCFs: Perform initial review for scope, attain sign-offs and justifications, set up review meetings, etc.
Maintain and review schedules/campaigns: Notify associated departments of deadlines and keep documents within their scheduled timeframe; begin building a deep understanding of how scheduling works; communicating to group and appropriate departments concerning schedules
Interested? What we need you to have: Degree in life sciences preferred
Several years of biotech or pharmaceutical manufacturing industry experience
Demonstrated document editing and proofreading experience
Adept at researching
Basic knowledge of cGMP and manufacturing process knowledge
Comprehend how CAPAs (corrective actions/preventative actions) and change controls must be incorporated into a document
Demonstrated proficiency in Microsoft Office Suite; particularly Word, Excel, and Project
Strong written and oral communication skills
Initiative to identify and address potential problems
Highly organized with effective time management (ensuring completion of work tasks)
Strong attention to detail.
Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.
Lonza. The place to Go, Stay and Grow.
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